FDA Inspection
Lisa M. Cibik, M.D.Lisa M. Cibik, M.D. – FDA Inspection, Nov 14, 2013
Record Details
This FDA Inspection record concerns Lisa M. Cibik, M.D., with an inspection on November 14, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lisa M. Cibik, M.D.
- Inspection Date
- November 14, 2013
- Product Type
- Devices
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ID · 0811966f-bcc3-4243-a225-2a954d44c9bf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 854685
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of Lisa M. Cibik, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 11, 2019 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Lisa M. Cibik, M.D.
- FDA Inspection 1107968 - 2019-10-11
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