FDA Inspection
3M Company3M Company – FDA Inspection, Apr 13, 2011
Record Details
This FDA Inspection record concerns 3M Company, with an inspection on April 13, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- 3M Company
- Inspection Date
- April 13, 2011
- Product Type
- Drugs
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ID · 6b4cdce7-911a-41d2-91fc-8d3441c86ce9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 720685
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.101(c)Weighing/measuring/subdividing supervision
- 21 CFR 211.115(a)Reprocessing procedures lack steps to be taken
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.192No written record of investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of 3M Company
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 22, 2022 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 19, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 5, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 5, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for 3M Company
- FDA Inspection 1182209 - 2022-09-22
- FDA Inspection 984843 - 2016-08-19
- FDA Inspection 787941 - 2012-06-05
- FDA Inspection 649164 - 2010-03-05
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