# FDA Inspection 600252 - Draeger, Inc. - July 09, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/draeger-inc/e226b3de-4efb-4752-bd4f-61ba92150e76
Source feed: FDA_Inspections

> FDA Inspection 600252 for Draeger, Inc. on July 09, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 600252
- Company Name: Draeger, Inc.
- Inspection Date: 2009-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/draeger-inc/6f523da8-ba13-46e1-8deb-9f23eef83af1

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