# DynaFlex - Inspection Records

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

> Inspection records and compliance data for DynaFlex in Lake Saint Louis, Missouri. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1305824 - DynaFlex - 2026-03-06](https://www.keypedia.com/records/fda_inspections/dynaflex/6ae6289c-2f61-4384-8686-e9dd947dc383) — 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](https://www.keypedia.com/records/fda_inspections/dynaflex/87fbdcca-c8d2-43c2-aa04-34aa1a4f1e15) — 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/0226fb05-c7a0-4f3a-a4db-17fc00be71c8) — classification: Voluntary Action Indicated (VAI), 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 1048804 - DynaFlex - 2018-04-18](https://www.keypedia.com/records/fda_inspections/dynaflex/58ec8dbe-230e-4113-924b-f8c2b0616a46) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2018
- [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

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## Related Officers

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