# FDA Inspection 1100886 - Collimare, LLC - August 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/collimare-llc/3de39359-be19-4496-95d5-aaa7b3e251c6
Source feed: FDA_Inspections

> FDA Inspection 1100886 for Collimare, LLC on August 14, 2019. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100886 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/collimare-llc/8b7e62d2-bdac-4cc8-b9f3-cc9c9b0f951e)
- [FDA Inspection 1100886 - 2019-08-14](https://www.keypedia.com/records/fda_inspections/collimare-llc/62e9c0c4-cecf-407f-bbe1-536bbe3e9458)
- [FDA Inspection 750110 - 2011-09-30](https://www.keypedia.com/records/fda_inspections/collimare-llc/cebed449-ad05-4434-9fde-24b221fae4e7)
- [FDA Inspection 555085 - 2008-12-09](https://www.keypedia.com/records/fda_inspections/collimare-llc/8118772f-ff3e-495a-b1f9-efff4b2541e9)
- [FDA Inspection 555085 - 2008-12-09](https://www.keypedia.com/records/fda_inspections/collimare-llc/4f8dbb2a-fde5-4e82-8726-aee16625b9ef)

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