FDA Inspection
Neal S. Kleiman, M.D.Neal S. Kleiman, M.D. – FDA Inspection, Dec 6, 2018
Record Details
This FDA Inspection record concerns Neal S. Kleiman, M.D., with an inspection on December 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6e7f99b8-b8f2-448f-8a8f-7fa8d00dd62e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1074202
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Neal S. Kleiman, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 26, 2013 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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