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FDA Inspection 1073392 — Merck Sharp & Dohme LLC

Merck Sharp & Dohme LLC — FEI 1112271

The FDA completed an inspection of Merck Sharp & Dohme LLC on October 26, 2018 in Elkton, VA. 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
October 26, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Elkton, VA (United States)

Facility

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  • 1094564 (VAI Fri Jun 28 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044990 (NAI Fri Jan 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources