FDA Inspection
Amit Mehta, MDAmit Mehta, MD – FDA Inspection, Aug 9, 2012
Record Details
This FDA Inspection record concerns Amit Mehta, MD, with an inspection on August 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Amit Mehta, MD
- Inspection Date
- August 9, 2012
- Product Type
- Devices
View Company Profile
ID · 1238a6b9-a50a-4bde-bfc4-b4274e52a0c6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 796202
- 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 56.115(a)(3)Records of continuing review
- 21 CFR 812.140(d)Record retention inadequate
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