FDA Inspection 1280306 — PML NYC, LLC

PML NYC, LLC — FEI 2430738

The FDA completed an inspection of PML NYC, LLC on September 25, 2025 in Long Island City, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Long Island City, NY (United States)

Citations

IDCFRDescription
202621 CFR 211.192Quality control unit review of records
360321 CFR 211.160(b)Scientifically sound laboratory controls
435221 CFR 211.160(b)(4)Calibration - at intervals, written program, remedial action