# FDA Inspection 797536 - Medgyn Products, Inc. - September 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/medgyn-products-inc/a94b53bd-2a76-444f-91b5-e851d6ddf556
Source feed: FDA_Inspections

> FDA Inspection 797536 for Medgyn Products, Inc. on September 06, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 797536
- Company Name: Medgyn Products, Inc.
- Inspection Date: 2012-09-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 903913 - 2014-10-15](https://www.keypedia.com/records/fda_inspections/medgyn-products-inc/eb413cbc-fdce-410e-b27c-b73e94f0517d)
- [FDA Inspection 797536 - 2012-09-06](https://www.keypedia.com/records/fda_inspections/medgyn-products-inc/e53fb0dc-67b1-4056-acec-9139ea8ca7ac)

Company: https://www.keypedia.com/companies/medgyn-products-inc/6a0e2271-24ca-4b71-872d-21bdaf40c19f

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