FDA Warning Letter — Re-Gen Active Lab Inc

Case 620763 — FEI 3015174203

The FDA took a Warning Letter action against Re-Gen Active Lab Inc on May 27, 2022 (Irving, TX). The action was issued by CBER and concerns biologics products. This facility has 1 recent FDA inspection on record.

Action details

Facility
Re-Gen Active Lab Inc
Date
May 27, 2022
Fiscal Year
2022
Product Type
Biologics
Center
CBER
Location
Irving, TX (United States)

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