FDA Inspection 1145211 — GREFI

GREFI — FEI 3004841580

The FDA completed an inspection of GREFI on June 14, 2021 in Ponce, PR. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 14, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Ponce, PR (United States)