# FDA Inspection 555085 - Collimare, LLC - December 09, 2008

Source: https://www.keypedia.com/records/fda_inspections/collimare-llc/8118772f-ff3e-495a-b1f9-efff4b2541e9
Source feed: FDA_Inspections

> FDA Inspection 555085 for Collimare, LLC on December 09, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 555085
- Company Name: Collimare, LLC
- Inspection Date: 2008-12-09
- 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.keypedia.com/companies/collimare-llc/5b4bd002-961c-429d-842a-c2e1fa0bffb8

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