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FDA Inspection 907330 — Cosmax USA, Corporation

Cosmax USA, Corporation — FEI 3002679704

The FDA completed an inspection of Cosmax USA, Corporation on December 22, 2014 in Carteret, 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
December 22, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carteret, NJ (United States)

Facility

Other inspections at this facility

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  • 1177107 (VAI Fri Jul 22 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1121022 (OAI Tue Mar 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099676 (NAI Thu Jul 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1025842 (VAI Wed Sep 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources