FDA Inspection 1122962 — Broekman Instituut B.V.

Broekman Instituut B.V. — FEI 3009390218

The FDA completed an inspection of Broekman Instituut B.V. on March 6, 2020 in Someren. 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
March 6, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Someren (Netherlands)