# FDA Inspection 1108239 - Gynie, Inc. - October 02, 2019

Source: https://www.keypedia.com/records/fda_inspections/gynie-inc/c807bc13-e206-4b87-9c91-840f174cd677
Source feed: FDA_Inspections

> FDA Inspection 1108239 for Gynie, Inc. on October 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1108239
- Company Name: Gynie, Inc.
- Inspection Date: 2019-10-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1108239 - 2019-10-02](https://www.keypedia.com/records/fda_inspections/gynie-inc/804b347f-01d8-4fb9-b90d-1f170b8fe109)

Company: https://www.keypedia.com/companies/gynie-inc/b5f58bb5-774a-4999-8cf7-1ac625ebdee2

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