FDA Inspection 907330 — Cosmax USA, Corporation

Cosmax USA, Corporation — FEI 3002679704

The FDA completed an inspection of Cosmax USA, Corporation on Dec 22, 2014 in Carteret, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 22, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carteret, NJ (United States)

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