FDA Inspection
DynaFlexDynaFlex – FDA Inspection, Apr 18, 2018
Record Details
This FDA Inspection record concerns DynaFlex, with an inspection on April 18, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d378f306-d988-4b09-abd8-9d63467ff896
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1048804
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of DynaFlex
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2026 | Not classified | Kansas City District Office | Compliance: Medical Devices |
| September 25, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 5, 2019 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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