# FDA Inspection 1265002 - WomanCare Global - March 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/womancare-global/3cd3b5e1-1b9b-4180-97b3-006617f7a27c
Source feed: FDA_Inspections

> FDA Inspection 1265002 for WomanCare Global on March 13, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1265002
- Company Name: WomanCare Global
- Inspection Date: 2025-03-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1265002 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/womancare-global/d683d610-96ce-4d65-83bc-c84254e408bf)
- [FDA Inspection 1265002 - 2025-03-13](https://www.keypedia.com/records/fda_inspections/womancare-global/92957cfb-369b-4eb7-bb75-c9987791531e)
- [FDA Inspection 788350 - 2012-06-15](https://www.keypedia.com/records/fda_inspections/womancare-global/90180952-81d2-4513-b14e-f4008e3e309f)

Company: https://www.keypedia.com/companies/womancare-global/3d58940b-24d0-4b2e-8a6c-db50adea3e09

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