FDA Inspection
Brooke R. Seckel, M.D.Brooke R. Seckel, M.D. – FDA Inspection, Feb 4, 2011
Record Details
This FDA Inspection record concerns Brooke R. Seckel, M.D., with an inspection on February 4, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Brooke R. Seckel, M.D.
- Inspection Date
- February 4, 2011
- Product Type
- Devices
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ID · 9a380363-5427-4513-9b35-6771240ed966
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 712684
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.140(a)(3)(iii)Investigator records of exposure to device inadequate
- 21 CFR 812.140(a)(1)Investigator correspondence records inadequate
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Other FDA inspections of Brooke R. Seckel, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 25, 2014 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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