# FDA Inspection 571101 - Peter Catalano, M.D. - March 17, 2009

Source: https://www.keypedia.com/records/fda_inspections/peter-catalano-md/06b1dbd0-008b-427d-bf86-86237b93de3a
Source feed: FDA_Inspections

> FDA Inspection 571101 for Peter Catalano, M.D. on March 17, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 571101
- Company Name: Peter Catalano, M.D.
- Inspection Date: 2009-03-17
- 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/peter-catalano-md/6cf282ec-8acf-4d8d-868e-e3f5d4bad4d4

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