FDA Inspection 1064581 - Avantor Inc. - August 03, 2018
FDA Inspection 1064581 for Avantor Inc. on August 03, 2018. Classification: No Action Indicated (NAI).
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FDA Inspection 1064581 for Avantor Inc. on August 03, 2018. Classification: No Action Indicated (NAI).
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Company
Avantor Inc.Inspection Date
August 3, 2018
Product Type
Drugs
ID: 5740f839-13ca-4930-9581-fd28747e01c7
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