FDA Inspection 1281580 — Cosmax USA, Corporation

Cosmax USA, Corporation — FEI 3002679704

The FDA completed an inspection of Cosmax USA, Corporation on Sep 12, 2025 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 12, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carteret, NJ (United States)

Citations

IDCFRDescription
192021 CFR 211.166(a)(3)Valid stability test methods

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