FDA Inspection
Manish Mehta, MDManish Mehta, MD – FDA Inspection, Jun 13, 2012
Record Details
This FDA Inspection record concerns Manish Mehta, MD, with an inspection on June 13, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Manish Mehta, MD
- Inspection Date
- June 13, 2012
- Product Type
- Devices
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ID · bc910349-8bcd-44ae-a34f-d92728607a1d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 787172
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Manish Mehta, MD
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 9, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 24, 2011 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Manish Mehta, MD
- FDA Inspection 913098 - 2015-02-06
- FDA Inspection 792362 - 2012-07-09
- FDA Inspection 750025 - 2011-10-24
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