FDA Inspection 1077526 — MP Biomedicals Asia Pacific Pte Ltd

MP Biomedicals Asia Pacific Pte Ltd — FEI 3008819649

The FDA completed an inspection of MP Biomedicals Asia Pacific Pte Ltd on December 14, 2018 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 14, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Singapore (Singapore)