FDA Inspection
Ramesh Hariharan, MDRamesh Hariharan, MD – FDA Inspection, Jun 17, 2014
Record Details
This FDA Inspection record concerns Ramesh Hariharan, MD, with an inspection on June 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ramesh Hariharan, MD
- Inspection Date
- June 17, 2014
- Product Type
- Devices
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ID · c0f2604a-f04c-42dc-8455-8f660129d806
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 885238
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
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Other FDA inspections of Ramesh Hariharan, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 9, 2021 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Ramesh Hariharan, MD
- FDA Inspection 1141316 - 2021-04-09
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