FDA Inspection
Manish Mehta, MDManish Mehta, MD – FDA Inspection, Oct 24, 2011
Record Details
This FDA Inspection record concerns Manish Mehta, MD, with an inspection on October 24, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Manish Mehta, MD
- Inspection Date
- October 24, 2011
- Product Type
- Devices
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ID · 1ba4faa4-0267-484b-8cd0-26466beb1039
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 750025
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.40Sponsors" general responsibilities
- 21 CFR 50.20Consent not obtained, exceptions do not apply
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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 |
| June 13, 2012 | VAI | 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 787172 - 2012-06-13
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