# Lisa M. Cibik, M.D. – FDA Inspection, Nov 14, 2013

Source: https://www.keypedia.com/records/fda_inspections/lisa-m-cibik-md/0811966f-bcc3-4243-a225-2a954d44c9bf
Source feed: FDA_Inspections

> FDA inspection 854685 of Lisa M. Cibik, M.D., November 14, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 854685
- Company Name: Lisa M. Cibik, M.D.
- Inspection Date: 2013-11-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1107968 - 2019-10-11

Company: https://www.keypedia.com/companies/lisa-m-cibik-md/0140722a-a07d-44c4-9080-3221e253fd13

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7