FDA Warning Letter — Genuine Virgin Aloe Corp

Case 679744 — FEI 3008235829

The FDA took a Warning Letter action against Genuine Virgin Aloe Corp on Jul 1, 2024 (Anaheim, CA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Genuine Virgin Aloe Corp
Date
Jul 1, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Anaheim, CA (United States)

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