# Dyn'r – FDA Inspection, Sep 13, 2018

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

> FDA inspection 1075894 of Dyn'r, September 13, 2018. Classification: No Action Indicated (NAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1263642 - 2025-02-06

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

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