# The Gillette Company – FDA Inspection, Oct 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/the-gillette-company/aa389093-6d98-4203-a458-9147a966724b
Source feed: FDA_Inspections

> FDA inspection 1030018 of The Gillette Company, October 26, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030018
- Company Name: The Gillette Company
- Inspection Date: 2017-10-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

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- FDA Inspection 611827 - 2009-09-16
- FDA Inspection 572521 - 2009-03-26

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christopher-d-leach/2a3c4b73-f082-4f33-aa2d-52d1abbb6d55)

Company: https://www.keypedia.com/companies/the-gillette-company/d06f81d4-486f-48cf-86f3-765f69bda9d4

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c