FDA Inspection 1278383 - Avista Pharma Solutions, Inc. dba Cambrex - July 25, 2025

FDA Inspection 1278383 for Avista Pharma Solutions, Inc. dba Cambrex on July 25, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1278383 for Avista Pharma Solutions, Inc. dba Cambrex on July 25, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.192

21 CFR 211.22(d)

21 CFR 211.56(a)

21 CFR 211.58

21 CFR 211.68(b)

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Record Information

Company

Avista Pharma Solutions, Inc. dba Cambrex

Inspection Date

July 25, 2025

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 49901d52-564d-4e1c-a292-69b90143b94a

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