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FDA Inspection 864565 — Garonit Pharmaceutical, Inc.

Garonit Pharmaceutical, Inc. — FEI 3003961853

The FDA completed an inspection of Garonit Pharmaceutical, Inc. on January 31, 2014 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
January 31, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fairfield, NJ (United States)

Facility

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FDA data resources