FDA Inspection 562521 — Draeger Medical Systems, Inc.
The FDA completed an inspection of Draeger Medical Systems, Inc. on Feb 12, 2009 in Telford, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Feb 12, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Telford, PA (United States)