# FDA Inspection 1075894 - Dyn'r - September 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/dynr/86c4ed47-a14e-4b8b-bf7c-e4bd17ad7c53
Source feed: FDA_Inspections

> FDA Inspection 1075894 for Dyn'r on September 13, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1075894
- Company Name: Dyn'r
- Inspection Date: 2018-09-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/dynr/54587a44-0d7a-4956-982c-d0c26877a040

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