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

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Record Details

This FDA Inspection record concerns Avista Pharma Solutions, Inc. dba Cambrex, with an inspection on July 25, 2025, issued by the New England District Office, covering human drugs.

Company: Avista Pharma Solutions, Inc. dba Cambrex
Inspection Date: July 25, 2025
Product Type: Human Drugs
Office: New England District Office

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ID · 07d264c9-9218-4fc2-92ce-25f1f2348432

Violation Codes5

21 CFR 211.19221 CFR 211.22(d)21 CFR 211.56(a)21 CFR 211.5821 CFR 211.68(b)

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