# FDA Inspection 1051610 - Femasys Inc. - February 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/femasys-inc/3693d3cf-89fc-4002-9ac9-cae827bfdd62
Source feed: FDA_Inspections

> FDA Inspection 1051610 for Femasys Inc. on February 14, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051610
- Company Name: Femasys Inc.
- Inspection Date: 2018-02-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1153124 - 2021-09-23](https://www.keypedia.com/records/fda_inspections/femasys-inc/4491f47d-0c82-4d48-9a16-a5feaf0abb04)
- [FDA Inspection 1051610 - 2018-02-14](https://www.keypedia.com/records/fda_inspections/femasys-inc/7abccc55-83a7-4de2-ba6d-2dacdf163073)

Company: https://www.keypedia.com/companies/femasys-inc/d1464805-ecbd-4e20-9568-63921fa30224

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