# FDA Inspection 1091481 - Med-Dyne, Inc. - May 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/med-dyne-inc/d17f9ef9-a330-4252-b4be-39686a34e1e3
Source feed: FDA_Inspections

> FDA Inspection 1091481 for Med-Dyne, Inc. on May 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091481
- Company Name: Med-Dyne, Inc.
- Inspection Date: 2019-05-21
- 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/med-dyne-inc/4137b0f6-2fbd-47e2-91b7-ad00ca650019

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