# George E Woodman M D – FDA Inspection, Aug 14, 2014

Source: https://www.keypedia.com/records/fda_inspections/george-e-woodman-m-d/d62c3608-38ae-4d0c-aca6-841a78b3c8fa
Source feed: FDA_Inspections

> FDA inspection 891483 of George E Woodman M D, August 14, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891483
- Company Name: George E Woodman M D
- Inspection Date: 2014-08-14
- 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: 1

## Related Documents

- FDA Inspection 1071207 - 2018-10-26
- FDA Inspection 675795 - 2010-07-15

Company: https://www.keypedia.com/companies/george-e-woodman-m-d/f12b469e-fa18-4c7f-94b1-51c98488f5ed

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