# FDA Inspection 916609 - Biegler GmbH - January 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/biegler-gmbh/8015fe87-e651-4394-9b23-2dc6fceb73e2
Source feed: FDA_Inspections

> FDA Inspection 916609 for Biegler GmbH on January 22, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916609
- Company Name: Biegler GmbH
- Inspection Date: 2015-01-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/biegler-gmbh/a51d97cb-1fbf-47b7-82e7-1cdc6f1fe04d

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