FDA Warning Letter — VITAMINVAPE INC

Case 617787 — FEI 3014219499

The FDA took a Warning Letter action against VITAMINVAPE INC on Dec 1, 2021 (Las Vegas, NV). The action was issued by CDER and concerns drugs products.

Action Details

Facility
VITAMINVAPE INC
Date
Dec 1, 2021
Fiscal Year
2022
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.