FDA Inspection 1241221 — Qualimax LLC

Qualimax LLC — FEI 3004599007

The FDA completed an inspection of Qualimax LLC on Jun 13, 2024 in Ridgefield, 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 13, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ridgefield, NJ (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
360321 CFR 211.160(b)Scientifically sound laboratory controls