FDA Inspection 835110 — Prothya Biosolutions Netherlands B.V.

Prothya Biosolutions Netherlands B.V. — FEI 3007166802

The FDA completed an inspection of Prothya Biosolutions Netherlands B.V. on Jun 4, 2013 in Amsterdam. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Biologics.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Jun 4, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Amsterdam (Netherlands)

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