FDA Inspection 981011 - Lonza Guangzhou Pharmaceutical Ltd. - August 19, 2016
FDA Inspection 981011 for Lonza Guangzhou Pharmaceutical Ltd. on August 19, 2016. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 981011 for Lonza Guangzhou Pharmaceutical Ltd. on August 19, 2016. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
August 19, 2016
Product Type
Drugs
ID: a82982c1-d7cb-469a-94fa-6d94ac953e3e
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