# Nugyn, Inc – FDA Inspection, Aug 2, 2017

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

> FDA inspection 1020397 of Nugyn, Inc, August 02, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 838407 - 2013-06-28
- FDA Inspection 683435 - 2010-09-01

## Related Officers

- Issuing Officer

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