# FDA Inspection 1277871 - Femcap Inc - August 08, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/b041ef66-61ed-4284-ad21-53b13183c227
Source feed: FDA_Inspections

> FDA Inspection 1277871 for Femcap Inc on August 08, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1277871
- Company Name: Femcap Inc
- Inspection Date: 2025-08-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1277871 - 2025-08-08](https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/55d7a96f-3621-4e33-939b-8480de59ffa4)
- [FDA Inspection 1277871 - 2025-08-08](https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/c1d6999d-e2ab-49fc-a2a5-2afb6c095945)
- [FDA Inspection 1277871 - 2025-08-08](https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/c13c16e1-508d-4ba3-a4ef-7631f48257a8)
- [FDA Inspection 837673 - 2013-06-26](https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/1c5674d5-4bca-40ed-a173-c83fe42d2f6e)
- [FDA Inspection 837673 - 2013-06-26](https://www.globalkeysolutions.net/records/fda_inspections/femcap-inc/351213fe-1671-4421-8046-660fd49bd5ac)

Company: https://www.globalkeysolutions.net/companies/femcap-inc/14e00c1f-7264-461e-a8ce-c517067305ec

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