# FDA Inspection 830902 - Unicare Biomedical, Inc. - May 09, 2013

Source: https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/e4739503-59ee-4ec5-a813-2704864fdce2
Source feed: FDA_Inspections

> FDA Inspection 830902 for Unicare Biomedical, Inc. on May 09, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 830902
- Company Name: Unicare Biomedical, Inc.
- Inspection Date: 2013-05-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1174261 - 2022-06-28](https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/7df62edb-0290-41a4-b706-8a6cd9aa3701)
- [FDA Inspection 1174261 - 2022-06-28](https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/e020cade-59a5-493c-ab0f-2c7dac482177)
- [FDA Inspection 1169384 - 2022-05-11](https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/0304e79e-9a21-486d-9300-386a60d54d34)
- [FDA Inspection 1169384 - 2022-05-11](https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/4a391768-3482-4465-8c46-8c39357598e5)
- [FDA Inspection 974365 - 2016-04-13](https://www.keypedia.com/records/fda_inspections/unicare-biomedical-inc/9e537a99-3818-43df-ac8d-ebfa7fdfc285)

Company: https://www.keypedia.com/companies/unicare-biomedical-inc/cc3f9395-4e68-436b-b11b-f80b725a903b

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