# Draeger, Inc. – FDA Inspection, Jul 9, 2009

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

> FDA inspection 600252 of Draeger, Inc., July 09, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1258491 - 2024-12-11
- [FDA Inspection 841213 - 2013-07-03](https://www.keypedia.com/records/fda_inspections/draeger-inc/ed3d3250-4974-40c0-b568-631b0957bbd7)

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

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