# FDA Inspection 805760 - VUMii, Inc. - October 31, 2012

Source: https://www.keypedia.com/records/fda_inspections/vumii-inc/a9ac7bbf-7f8d-4f0b-9599-b5ef488d0537
Source feed: FDA_Inspections

> FDA Inspection 805760 for VUMii, Inc. on October 31, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 805760
- Company Name: VUMii, Inc.
- Inspection Date: 2012-10-31
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/vumii-inc/a7c91774-2ded-49a7-b8a1-a35040b60cd0

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