FDA Warning Letter — One Way Drug, LLC

Case 573455 — FEI 3010839113

The FDA took a Warning Letter action against One Way Drug, LLC on Mar 14, 2019 (Las Vegas, NV). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
One Way Drug, LLC
Date
Mar 14, 2019
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Las Vegas, NV (United States)

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