# DynaFlex – FDA Inspection, Mar 6, 2026

Source: https://www.keypedia.com/records/fda_inspections/dynaflex/9f9a3483-b6d0-4be9-a38f-109970e27856
Source feed: FDA_Inspections

> FDA inspection 1305824 of DynaFlex, March 06, 2026. 6 citations under 21 CFR parts 801 and 803. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1305824
- Company Name: DynaFlex
- Inspection Date: 2026-03-06
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Kansas City District Office
- Citation Count: 6

## Related Documents

- [FDA Inspection 1218587 - 2023-09-25](https://www.keypedia.com/records/fda_inspections/dynaflex/f73cc413-96b2-4adc-ad9e-f84ea9421dc5)
- [FDA Inspection 1102731 - 2019-09-05](https://www.keypedia.com/records/fda_inspections/dynaflex/c9771b96-b6ae-4cb5-9c2e-cb3f1971939f)
- [FDA Inspection 1048804 - 2018-04-18](https://www.keypedia.com/records/fda_inspections/dynaflex/d378f306-d988-4b09-abd8-9d63467ff896)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)

Company: https://www.keypedia.com/companies/dynaflex/a805d418-c220-4dcf-8f82-08ee4c075100

Office: https://www.keypedia.com/offices/kansas-city-district-office/cd397ab1-df4e-46f1-ab1c-0f6db9abcf79