FDA Warning Letter — Vevazz LLC

Case 592118 — FEI 3009690171

The FDA took a Warning Letter action against Vevazz LLC on Dec 26, 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
Vevazz LLC
Date
Dec 26, 2019
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Dallas, TX (United States)

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