FDA Inspection
John D. Hummel, M.D.John D. Hummel, M.D. – FDA Inspection, Jun 11, 2010
Record Details
This FDA Inspection record concerns John D. Hummel, M.D., with an inspection on June 11, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- John D. Hummel, M.D.
- Inspection Date
- June 11, 2010
- Product Type
- Devices
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ID · bbd92269-06d1-47f0-abfe-eae750a8f82a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663983
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of John D. Hummel, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 25, 2023 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for John D. Hummel, M.D.
- FDA Inspection 1217141 - 2023-08-25
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