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FDA Inspection 986872 — Garonit Pharmaceutical, Inc.

Garonit Pharmaceutical, Inc. — FEI 3003961853

The FDA completed an inspection of Garonit Pharmaceutical, Inc. on August 26, 2016 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: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 26, 2016
Fiscal Year
2016
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Fairfield, NJ (United States)

Facility

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  • 1116449 (VAI Tue Jan 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1035090 (NAI Tue Nov 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 864565 (VAI Fri Jan 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 718283 (NAI Mon Apr 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources