FDA Inspection
3M COMPANY3M COMPANY – FDA Inspection, May 25, 2018
Record Details
This FDA Inspection record concerns 3M COMPANY, with an inspection on May 25, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · cb4c3411-7dfc-4560-83cc-1b8f44c96633
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1060963
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 211.84(d)(1)Component identity verification
- 21 CFR 211.68(b)input/output verification
- 21 CFR 211.194(a)(4)Complete Test Data
- 21 CFR 211.22(d)Procedures not in writing, fully followed
Full citation text and observation details available on the Dashboard.
Other FDA inspections of 3M COMPANY
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 8, 2017 | Not classified | Minneapolis District Office | |
| December 5, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 27, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for 3M COMPANY
- FDA Inspection 1039481 - 2017-06-08
- FDA Inspection 813433 - 2012-12-05
- FDA Inspection 660586 - 2010-04-27
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