FDA Inspection 1002457 — 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 Nov 7, 2016 in Singapore. 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). Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 7, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Singapore (Singapore)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.