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FDA Inspection
•N.V. Organon (MSD)•November 7, 2017

N.V. Organon (MSD) – FDA Inspection, Nov 7, 2017

Record Details

This FDA Inspection record concerns N.V. Organon (MSD), with an inspection on November 7, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
N.V. Organon (MSD)
Inspection Date
November 7, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Reyes Candau-Chacon (Issuing Officer)
View Company Profile

ID · c913b5eb-29c4-42d5-885b-759d02803db9

Inspection Facts

Inspection number
1037871
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of N.V. Organon (MSD)

11
DateClassificationOfficeProject area
September 8, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 20, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 10, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 7, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 11 other inspections on the company page
Other documents for N.V. Organon (MSD)
  • FDA Inspection 1248564 - 2022-09-08
  • FDA Inspection 1271522 - 2022-08-25
  • FDA Inspection 1109695 - 2019-09-20
  • FDA Inspection 1123556 - 2019-09-10
  • FDA Inspection 1031159 - 2017-09-07

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