FDA Inspection
Mission Systems Davenport Inc.Mission Systems Davenport Inc. – FDA Inspection, Aug 12, 2009
Record Details
This FDA Inspection record concerns Mission Systems Davenport Inc., with an inspection on August 12, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 12, 2009
- Product Type
- Devices
View Company Profile
ID · 5562c915-d23a-443a-89ca-434d571e8041
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 607226
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.100(b)Documentation
- 21 CFR 820.20Management responsibility
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.30(b)Design plans - Lack of or inadequate
- 21 CFR 820.30(e)Design review - documentation
- 21 CFR 820.30(g)Design validation - documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Mission Systems Davenport Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 30, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 11, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 11, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mission Systems Davenport Inc.
- FDA Inspection 1202012 - 2023-03-30
- FDA Inspection 992396 - 2016-10-11
- FDA Inspection 738855 - 2011-08-11
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