FDA Inspection 934887 — PML NYC, LLC

PML NYC, LLC — FEI 2430738

The FDA completed an inspection of PML NYC, LLC on Jul 10, 2015 in Long Island City, NY. 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). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Long Island City, NY (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
356521 CFR 211.58Buildings not maintained in good state of repair
434221 CFR 211.142(b)Storage under appropriate conditions

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.