# FDA Inspection 1048581 - Curae'Lase, Inc. - February 05, 2018

Source: https://www.keypedia.com/records/fda_inspections/curaelase-inc/e23a7b4c-05cb-4f8f-a6d2-e6e3f1aa0aba
Source feed: FDA_Inspections

> FDA Inspection 1048581 for Curae'Lase, Inc. on February 05, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048581
- Company Name: Curae'Lase, Inc.
- Inspection Date: 2018-02-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 811634 - 2012-11-06](https://www.keypedia.com/records/fda_inspections/curaelase-inc/a2650ae1-b43a-40b9-9cea-d3ecbd18d031)
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Company: https://www.keypedia.com/companies/curaelase-inc/3a447af7-5ca6-4fc1-ae50-061fe35c0a34

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