FDA Inspection
Neal S. Kleiman, M.D.Neal S. Kleiman, M.D. – FDA Inspection, Nov 26, 2013
Record Details
This FDA Inspection record concerns Neal S. Kleiman, M.D., with an inspection on November 26, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neal S. Kleiman, M.D.
- Inspection Date
- November 26, 2013
- Product Type
- Devices
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ID · e4c22842-c6e7-49fd-acd6-746aa6e73a71
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 856696
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(1)Investigator correspondence records inadequate
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Other FDA inspections of Neal S. Kleiman, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 6, 2018 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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