FDA Inspection
DiaPharma Group IncDiaPharma Group Inc – FDA Inspection, Apr 29, 2022
Record Details
This FDA Inspection record concerns DiaPharma Group Inc, with an inspection on April 29, 2022, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DiaPharma Group Inc
- Inspection Date
- April 29, 2022
- Product Type
- Devices
View Company Profile
ID · b493f4de-ab73-489d-acc0-f6ce6e28fda6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1171225
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of DiaPharma Group Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 25, 2026 | Not classified | Cincinnati District Office | |
| August 31, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 11, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 8, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for DiaPharma Group Inc
- FDA Inspection 1306606 - 2026-02-25
- FDA Inspection 940414 - 2015-08-31
- FDA Inspection 749173 - 2011-10-11
- FDA Inspection 712065 - 2011-03-08
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