FDA Inspection 1225674 — Allen Cohn

Allen Cohn — FEI 3008043368

The FDA completed an inspection of Allen Cohn on December 15, 2023 in Denver, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 15, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Denver, CO (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
738421 CFR 50.25(b)(1)Statement of risks
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance