# FDA Inspection 661333 - UltiMed, Inc. - April 29, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/ultimed-inc/dff9852f-d4fc-486c-97e4-2ce29abb7969
Source feed: FDA_Inspections

> FDA Inspection 661333 for UltiMed, Inc. on April 29, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 661333
- Company Name: UltiMed, Inc.
- Inspection Date: 2010-04-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/ultimed-inc/48f43fcc-d123-4923-b6aa-583ed39a1f27

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