FDA Inspection
Grimm Scientific IndustriesGrimm Scientific Industries – FDA Inspection, Jun 16, 2023
Record Details
This FDA Inspection record concerns Grimm Scientific Industries, with an inspection on June 16, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 0ead4a99-705f-46b7-a41f-906ddeb5d9a6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1208256
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Grimm Scientific Industries
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 18, 2026 | VAI | Cincinnati District Office | Compliance: Devices |
| January 13, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 2, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Grimm Scientific Industries
- FDA Inspection 1336538 - 2026-09-18
- FDA Inspection 1000600 - 2017-01-13
- FDA Inspection 850525 - 2013-08-29
- FDA Inspection 771780 - 2012-03-02
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