# FDA Inspection 1048804 - DynaFlex - April 18, 2018

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

> FDA Inspection 1048804 for DynaFlex on April 18, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7