FDA Inspection 1209320 — Garonit Pharmaceutical, Inc.

Garonit Pharmaceutical, Inc. — FEI 3003961853

The FDA completed an inspection of Garonit Pharmaceutical, Inc. on July 6, 2023 in Fairfield, NJ. 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
July 6, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fairfield, NJ (United States)