# FDA Inspection 620283 - Provotec GmbH - September 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/provotec-gmbh/23a684b9-1fb0-4149-8cad-0a29b72324c3
Source feed: FDA_Inspections

> FDA Inspection 620283 for Provotec GmbH on September 25, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 620283
- Company Name: Provotec GmbH
- Inspection Date: 2009-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/provotec-gmbh/ab394caf-563f-46da-bbbc-566d9e51e831

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