FDA Inspection 666815 — Metro Med LLC

Metro Med LLC — FEI 3007380379

The FDA completed an inspection of Metro Med LLC on Jun 4, 2010 in Annapolis, MD. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 4, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Annapolis, MD (United States)

Citations

IDCFRDescription
1233621 CFR 1271.180(a)Procedures to meet core CTGP
1241521 CFR 1271.260(e)Temperature limits