# FDA Inspection 849682 - Alexander G Digenis MD - September 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/alexander-g-digenis-md/772e4709-acb1-49c0-ada8-96e062e7c3f4
Source feed: FDA_Inspections

> FDA Inspection 849682 for Alexander G Digenis MD on September 05, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 849682
- Company Name: Alexander G Digenis MD
- Inspection Date: 2013-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/alexander-g-digenis-md/02ac87dc-5e69-41d7-98ce-8b7f792a2f5d

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