# FDA Inspection 585862 - Femcare, Ltd. - May 21, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/femcare-ltd/7f6989e2-aedb-4d8e-97a8-c417213a69f2
Source feed: FDA_Inspections

> FDA Inspection 585862 for Femcare, Ltd. on May 21, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 585862
- Company Name: Femcare, Ltd.
- Inspection Date: 2009-05-21
- 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 585862 - 2009-05-21](https://www.globalkeysolutions.net/records/fda_inspections/femcare-ltd/cb755f1c-19d2-4197-93dd-ce780a224054)
- [FDA Inspection 585862 - 2009-05-21](https://www.globalkeysolutions.net/records/fda_inspections/femcare-ltd/84dc293e-6c12-4b7d-bc37-1ac376958cf4)

Company: https://www.globalkeysolutions.net/companies/femcare-ltd/a4e09802-8bf6-4579-bc48-ecc63d251b9e

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