FDA Warning Letter — Broncolin, S.A. de C.V.

Case 609329 — FEI 3009331372

The FDA took a Warning Letter action against Broncolin, S.A. de C.V. on December 21, 2020 (Ciudad De Mexico, Mexico). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Broncolin, S.A. de C.V.
Date
December 21, 2020
Fiscal Year
2021
Product Type
Drugs
Center
CDER
Location
Ciudad De Mexico (Mexico)