FDA Inspection
Jaafer Golzar, MDJaafer Golzar, MD – FDA Inspection, Jul 6, 2018
Record Details
This FDA Inspection record concerns Jaafer Golzar, MD, with an inspection on July 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Shalonda C. Clifford (Issuing Officer)
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ID · adf7880f-5efd-4b8f-acaa-d0dcce872f1c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1058653
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(d)Record retention inadequate
- 21 CFR 812.140(a)(3)Investigator's subject records inadequate
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