FDA Inspection 1102522 — GCAM Inc

GCAM Inc — FEI 3006805873

The FDA completed an inspection of GCAM Inc on September 16, 2019 in Moreno Valley, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Moreno Valley, CA (United States)

Citations

IDCFRDescription
1810721 CFR 630.15(b)(2)(iii)Donor consent clear