FDA Inspection
Kerendi Faraz, MDKerendi Faraz, MD – FDA Inspection, May 25, 2017
Record Details
This FDA Inspection record concerns Kerendi Faraz, MD, with an inspection on May 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 61007ae2-26fc-4442-9c66-e2f5a5339729
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1011987
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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