FDA Inspection
Fischer Medical Technologies, Inc.Fischer Medical Technologies, Inc. – FDA Inspection, Jun 5, 2009
Record Details
This FDA Inspection record concerns Fischer Medical Technologies, Inc., with an inspection on June 5, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 5, 2009
- Product Type
- Devices
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ID · df588e99-d319-4451-8d7c-44203b70e75c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 587950
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 820.198(a)(3)Processing MDRs {see also 803, 804}
- 21 CFR 820.100(a)(1)Analysis of data/reports from data sources
- 21 CFR 820.70(a)Production processes
- 21 CFR 820.30(g)Design validation - simulated testing
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Fischer Medical Technologies, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Fischer Medical Technologies, Inc.
- FDA Inspection 827080 - 2013-04-11
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