# FDA Inspection 606001 - Dr. Peter Levanovich - August 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/dr-peter-levanovich/11c0ee21-dec4-4a51-ad44-4d72b158f9d9
Source feed: FDA_Inspections

> FDA Inspection 606001 for Dr. Peter Levanovich on August 14, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 606001
- Company Name: Dr. Peter Levanovich
- Inspection Date: 2009-08-14
- 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/dr-peter-levanovich/b4ee89d1-f61a-4241-b3dc-7aedfee77588

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