# FDA Inspection 617850 - Edward D. Verrier, MD - September 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/edward-d-verrier-md/f0d9c59b-7b04-41fb-90ac-7d6d77627843
Source feed: FDA_Inspections

> FDA Inspection 617850 for Edward D. Verrier, MD on September 02, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 617850
- Company Name: Edward D. Verrier, MD
- Inspection Date: 2009-09-02
- 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/edward-d-verrier-md/8ff21f59-fb19-46d0-a9df-3e2f9ac2f8fd

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