FDA Inspection
Robert Cywes, M.D.Robert Cywes, M.D. – FDA Inspection, May 1, 2013
Record Details
This FDA Inspection record concerns Robert Cywes, M.D., with an inspection on May 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Robert Cywes, M.D.
- Inspection Date
- May 1, 2013
- Product Type
- Devices
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ID · 68a8c3fb-1ef8-4774-a724-6c33a87062f8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 830698
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of Robert Cywes, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 9, 2011 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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