# Collimare, LLC – FDA Inspection, Aug 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/collimare-llc/8b7e62d2-bdac-4cc8-b9f3-cc9c9b0f951e
Source feed: FDA_Inspections

> FDA inspection 1100886 of Collimare, LLC, August 14, 2019. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100886
- Company Name: Collimare, LLC
- Inspection Date: 2019-08-14
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 750110 - 2011-09-30
- FDA Inspection 555085 - 2008-12-09

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

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