FDA Inspection
N.V. Organon (MSD)N.V. Organon (MSD) – FDA Inspection, Sep 7, 2017
Record Details
This FDA Inspection record concerns N.V. Organon (MSD), with an inspection on September 7, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 4bcfe6d3-c3b4-4d49-b288-b8d6bad0d4ea
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031159
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of N.V. Organon (MSD)
11| Date | Classification | Office | Project area |
|---|---|---|---|
| September 8, 2022 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 25, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 20, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 10, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 7, 2017 | Not classified | Office of Inspections and Investigations |
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 1037871 - 2017-11-07
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