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   <title>Form  6-K        Alvotech                  For: Jul 29</title>
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   <pubDate>Wed, 29 Jul 2026 11:00:00 -0400</pubDate>
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   <title>Form  6-K        Alvotech                  For: Jul 29</title>
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   <title>FDA closes inspection of Alvotech's Iceland facility with VAI rating</title>
   <link>http://www.streetinsider.com/Corporate+News/FDA+closes+inspection+of+Alvotech%27s+Iceland+facility+with+VAI+rating/26831871.html</link>
   <description>&lt;p&gt;Alvotech (NASDAQ: ALVO) announced that the U.S. Food and Drug Administration has closed its inspection of the company's manufacturing facility in Reykjavik, Iceland, with a classification of Voluntary Action Indicated (VAI). The inspection was conducted in May 2026.&lt;/p&gt;&lt;p&gt;A VAI classification indicates that the FDA found objectionable conditions or practices, but the agency is not prepared to take or recommend any administrative or regulatory action.&lt;/p&gt;&lt;p&gt;&quot;This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing operations,&quot; said Lisa Graver, CEO of Alvotech. &quot;We continue to work with the</description>
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   <pubDate>Wed, 29 Jul 2026 09:26:28 -0400</pubDate>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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   <title>Alvotech announces successful closure of FDA inspection of manufacturing facility</title>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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&lt;p align=&quot;left&quot;&gt;REYKJAVIK, Iceland, July  29, 2026  (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO; ALVO-SDB) (the “Company”), a global biotechnology company specializing in the development and manufacture of biosimilar medicines for patients worldwide, today announced that the U.S. Food and Drug Administration (FDA) has closed its inspection of the company’s manufacturing facility in Reykjavik, Iceland, conducted in May 2026. The FDA has confirmed the inspection classification of the manufacturing site is Voluntary Action Indicated (VAI).&lt;/p&gt;  &lt;p&gt;“This is an important milestone for Alvotech and reflects the significant work our teams have undertaken to further strengthen our quality systems and manufacturing</description>
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