# DynaFlex, Lake Saint Louis, MO – FDA Inspections

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

> Inspection records and compliance data for DynaFlex in Lake Saint Louis, Missouri. 4 FDA inspections on record, 4 Form 483s, last inspected March 06, 2026.

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## Details

- Name: DynaFlex
- FEI Number: 1937100
- Address Line 1: 8050 Hawk Ridge Trl
- City: Lake Saint Louis
- State: Missouri
- Zip Code: 63367
- Country Name: United States
- Address: 8050 Hawk Ridge Trl, Lake Saint Louis, Missouri 63367, United States
- Country: United States

## Related Documents

- [483 - DynaFlex - 2026-03-06](https://www.keypedia.com/records/483/dynaflex/13ce12c6-cbe3-49a6-904c-0ca5dbf3947a) — source: FDA, date: March 6, 2026
- FDA Inspection 1305824 - DynaFlex - 2026-03-06 — source: FDA, date: March 6, 2026
- [FDA Inspection 1305824 - DynaFlex - 2026-03-06](https://www.keypedia.com/records/fda_inspections/dynaflex/9f9a3483-b6d0-4be9-a38f-109970e27856) — source: FDA, date: March 6, 2026
- [483 - DynaFlex - 2023-09-25](https://www.keypedia.com/records/483/dynaflex/156f620d-b36e-4ab3-b744-bb1a5d0356c4) — source: FDA, date: September 25, 2023
- [FDA Inspection 1218587 - DynaFlex - 2023-09-25](https://www.keypedia.com/records/fda_inspections/dynaflex/f73cc413-96b2-4adc-ad9e-f84ea9421dc5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2023
- FDA Inspection 1218587 - DynaFlex - 2023-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2023
- [483 - DynaFlex - 2019-09-05](https://www.keypedia.com/records/483/dynaflex/06413c35-a161-4932-8166-3c7e07c9715b) — source: FDA, date: September 5, 2019
- [FDA Inspection 1102731 - DynaFlex - 2019-09-05](https://www.keypedia.com/records/fda_inspections/dynaflex/c9771b96-b6ae-4cb5-9c2e-cb3f1971939f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 5, 2019
- FDA Inspection 1102731 - DynaFlex - 2019-09-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 5, 2019
- [FDA Inspection 1048804 - DynaFlex - 2018-04-18](https://www.keypedia.com/records/fda_inspections/dynaflex/d378f306-d988-4b09-abd8-9d63467ff896) — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2018
- FDA Inspection 1048804 - DynaFlex - 2018-04-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2018

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