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FDA Inspection
•Mission Systems Davenport Inc.•March 30, 2023

Mission Systems Davenport Inc. – FDA Inspection, Mar 30, 2023

Record Details

This FDA Inspection record concerns Mission Systems Davenport Inc., with an inspection on March 30, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
Mission Systems Davenport Inc.
Inspection Date
March 30, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Clifford F. Long (Issuing Officer)
View Company Profile

ID · a90f0287-842b-4e6d-9662-a6fc32bce06e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1202012
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 820.184(f)DHR - UDI not included

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Mission Systems Davenport Inc.

3
DateClassificationOfficeProject area
October 11, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
August 11, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
August 12, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Mission Systems Davenport Inc.
  • FDA Inspection 992396 - 2016-10-11
  • FDA Inspection 738855 - 2011-08-11
  • FDA Inspection 607226 - 2009-08-12

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