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FDA Inspection
•Merck & Co. Inc•November 19, 2015

Merck & Co. Inc – FDA Inspection, Nov 19, 2015

Record Details

This FDA Inspection record concerns Merck & Co. Inc, with an inspection on November 19, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Merck & Co. Inc
Inspection Date
November 19, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 2c87b1da-7191-4360-8d95-7a6f6181814a

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
955689
FDA center
Human Drugs
Project area
Bioresearch Monitoring

FDA Citations

3
  1. 21 CFR 312.50General responsibilities of sponsors
  2. 21 CFR 312.50Ensuring compliance with plan and protocol
  3. 21 CFR 312.57(c)Record retention requirement

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Merck & Co. Inc

15
DateClassificationOfficeProject area
August 14, 2026Not classifiedNew Jersey District Office
March 13, 2026Not classifiedNew Jersey District Office
December 18, 2025Not classifiedNew Jersey District Office
May 16, 2025Not classifiedNew Jersey District Office
March 27, 2025Not classifiedNew Jersey District Office
View all 15 other inspections on the company page
Other documents for Merck & Co. Inc
  • FDA Inspection 1329118 - 2026-08-14
  • FDA Inspection 1305632 - 2026-03-13
  • FDA Inspection 1283890 - 2025-12-18
  • FDA Inspection 1262774 - 2025-05-16
  • FDA Inspection 1264192 - 2025-03-27

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