# Med-Dyne, Inc. – FDA Inspection, Nov 1, 2016

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

> FDA inspection 999363 of Med-Dyne, Inc., November 01, 2016. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [Investigator](https://www.keypedia.com/people/shannon-a-gregory/3e791321-dced-4e1d-89a1-3da91d577961)

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