# FDA Inspection 891483 - George E Woodman M D - August 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 for George E Woodman M D on August 14, 2014. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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