# DynaFlex – FDA Inspection, Apr 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/dynaflex/d378f306-d988-4b09-abd8-9d63467ff896
Source feed: FDA_Inspections

> FDA inspection 1048804 of DynaFlex, April 18, 2018. Classification: No Action Indicated (NAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048804
- Company Name: DynaFlex
- Inspection Date: 2018-04-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- [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)

## 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/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7