FDA Inspection 769845 — Glasir Medical, LP

Glasir Medical, LP — FEI 3007789227

The FDA completed an inspection of Glasir Medical, LP on February 29, 2012 in San Antonio, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 29, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Antonio, TX (United States)

Citations

IDCFRDescription
1233621 CFR 1271.180(a)Procedures to meet core CTGP
1241621 CFR 1271.260(e)Storage temperatures recorded, maintained
1243321 CFR 1271.265(f)Return to inventory--procedures
1245721 CFR 1271.320(a)Procedures re complaints