FDA Inspection
The Gillette CompanyThe Gillette Company – FDA Inspection, Oct 26, 2017
Record Details
This FDA Inspection record concerns The Gillette Company, with an inspection on October 26, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · aa389093-6d98-4203-a458-9147a966724b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030018
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of The Gillette Company
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 24, 2026 | Not classified | Chicago District Office | |
| June 30, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 16, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 26, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for The Gillette Company
- FDA Inspection 1314592 - 2026-03-24
- FDA Inspection 732489 - 2011-06-30
- FDA Inspection 611827 - 2009-09-16
- FDA Inspection 572521 - 2009-03-26
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