# FDA Inspection 1020397 - Nugyn, Inc - August 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/nugyn-inc/693da43f-6f8c-434a-8151-15abe2f26815
Source feed: FDA_Inspections

> FDA Inspection 1020397 for Nugyn, Inc on August 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020397
- Company Name: Nugyn, Inc
- Inspection Date: 2017-08-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838407 - 2013-06-28](https://www.keypedia.com/records/fda_inspections/nugyn-inc/257cd54b-d627-47b8-8b0d-0a97bd2d3089)
- [FDA Inspection 683435 - 2010-09-01](https://www.keypedia.com/records/fda_inspections/nugyn-inc/b8910f9d-499a-4779-8b66-b64950d83b9d)

Company: https://www.keypedia.com/companies/nugyn-inc/4bf1b2ff-09de-4331-9075-491b3dc421cf

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