# FDA Inspection 999363 - Med-Dyne, Inc. - November 01, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/med-dyne-inc/fc6517d4-a81f-40cd-95ef-f6179200639e/
Source feed: FDA_Inspections

> FDA Inspection 999363 for Med-Dyne, Inc. on November 01, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999363
- Company Name: Med-Dyne, Inc.
- Inspection Date: 2016-11-01
- 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/med-dyne-inc/4137b0f6-2fbd-47e2-91b7-ad00ca650019

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