FDA Inspection 1023619 — Merck Sharp & Dohme BV

Merck Sharp & Dohme BV — FEI 3002807658

The FDA completed an inspection of Merck Sharp & Dohme BV on July 28, 2017 in Haarlem. 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
July 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Haarlem (Netherlands)