# FDA Inspection 629622 - UMI Intl - November 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/umi-intl/8d25fd60-3bb1-4cdb-a5d5-59cbc7348acf
Source feed: FDA_Inspections

> FDA Inspection 629622 for UMI Intl on November 18, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 629622
- Company Name: UMI Intl
- Inspection Date: 2009-11-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/umi-intl/d4483a5a-eb89-4dd6-825c-e4dea4481e8a

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