FDA Inspection 1088914 — Merck S.L.

Merck S.L. — FEI 3002649889

The FDA completed an inspection of Merck S.L. on May 31, 2018 in Mollet Del Valles. 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
May 31, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mollet Del Valles (Spain)

Additional Details

Mutual Recognition Agreement (MRA)