FDA Inspection 1229754 — Accugen Laboratories, Inc.

Accugen Laboratories, Inc. — FEI 3003286168

The FDA completed an inspection of Accugen Laboratories, Inc. on Feb 13, 2024 in Addison, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 13, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Addison, IL (United States)

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