FDA Inspection 1234429 — Merck Biodevelopment

Merck Biodevelopment — FEI 3009563840

The FDA completed an inspection of Merck Biodevelopment on December 4, 2020 in Martillac. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 4, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Martillac (France)

Additional Details

Mutual Recognition Agreement (MRA)