FDA Inspection 1023619 — Merck Sharp & Dohme BV

Merck Sharp & Dohme BV — FEI 3002807658

The FDA completed an inspection of Merck Sharp & Dohme BV on Jul 28, 2017 in Haarlem. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Haarlem (Netherlands)

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