FDA Inspection 997568 — Grifols BioSupplies Inc.

Grifols BioSupplies Inc. — FEI 3006118943

The FDA completed an inspection of Grifols BioSupplies Inc. on Dec 14, 2016 in Vista, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 14, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Vista, CA (United States)

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