FDA Warning Letter — Liveyon Labs Inc

Case 588399 — FEI 3015381220

The FDA took a Warning Letter action against Liveyon Labs Inc on December 5, 2019 (Yorba Linda, CA). The action was issued by CBER and concerns biologics products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Liveyon Labs Inc
Date
December 5, 2019
Fiscal Year
2020
Product Type
Biologics
Center
CBER
Location
Yorba Linda, CA (United States)