FDA Inspection
Brijeshwar S. Maini, M.D.Brijeshwar S. Maini, M.D. – FDA Inspection, Jun 30, 2017
Record Details
This FDA Inspection record concerns Brijeshwar S. Maini, M.D., with an inspection on June 30, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c238225b-9be0-4ab8-8467-dbd1a36d64e5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1020607
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(3)Investigator's subject records inadequate
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Other FDA inspections of Brijeshwar S. Maini, M.D.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 30, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 30, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Brijeshwar S. Maini, M.D.
- FDA Inspection 694684 - 2010-09-30
- FDA Inspection 683381 - 2010-09-30
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