FDA Inspection
3M Company IRB3M Company IRB – FDA Inspection, Apr 14, 2017
Record Details
This FDA Inspection record concerns 3M Company IRB, with an inspection on April 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b9415df1-bc34-41ae-a89d-40a57f8182a5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1010680
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 56.111(c)Children as subjects
- 21 CFR 56.108(a)(1)Initial and continuing reviews
- 21 CFR 56.108(b)(2)Prompt reporting of noncompliance
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Other FDA inspections of 3M Company IRB
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 7, 2025 | NAI | Bioresearch Monitoring | |
| October 10, 2012 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for 3M Company IRB
- FDA Inspection 1266843 - 2025-04-07
- FDA Inspection 803442 - 2012-10-10
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