# Curae'Lase, Inc. – FDA Inspection, Feb 5, 2018

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

> FDA inspection 1048581 of Curae'Lase, Inc., February 05, 2018. 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: 1048581
- Company Name: Curae'Lase, Inc.
- Inspection Date: 2018-02-05
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 811634 - 2012-11-06
- [FDA Inspection 718668 - 2011-04-07](https://www.keypedia.com/records/fda_inspections/curaelase-inc/6424adfc-861e-4b54-8b25-4dfc8b3692d3)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/miaja-umaedi/0a41661f-08bb-4523-ab09-b17e230068e0)

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