FDA Inspection
Zafar Jamil MdZafar Jamil Md – FDA Inspection, Jan 10, 2011
Record Details
This FDA Inspection record concerns Zafar Jamil Md, with an inspection on January 10, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Zafar Jamil Md
- Inspection Date
- January 10, 2011
- Product Type
- Devices
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ID · b527e008-e8e6-4620-99ea-dcbe864e7f92
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 707295
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
7- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(4)Investigator protocol records inadequate
- 21 CFR 812.100Investigator lack of control of investigational devices
- 21 CFR 50.27(a)Consent form not approved/signed/dated
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(2)(ii)Investigator records of persons receiving devices inadequate
- 21 CFR 812.140(a)(1)Investigator correspondence records inadequate
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