FDA Inspection 1229754 — Accugen Laboratories, Inc.

Accugen Laboratories, Inc. — FEI 3003286168

The FDA completed an inspection of Accugen Laboratories, Inc. on February 13, 2024 in Addison, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

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