Home / Compliance actions / 593692

FDA Warning Letter — CureWave Lasers, LLC

Case 593692 — FEI 3014268427

The FDA took a Warning Letter action against CureWave Lasers, LLC on Dec 12, 2019 (Dallas, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
CureWave Lasers, LLC
Date
Dec 12, 2019
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Dallas, TX (United States)

Facility

Recent inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.