Drug factory · FDA FEI 1000508879

Ajinomoto do Brasil Industria e Comercio de Alimentos Ltda.

ROD ANHANGUERA NÚMERO S/N COMPLEMENTO KM 131 DO JAGUARI, Limeira, Brazil

Brazil: 1

Problems found, fixed voluntarily at FDA's last inspection, Aug 11, 2023.

Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.

3 drug inspections on record since 2014: 0 with no problems, 3 with problems fixed voluntarily, 0 with FDA action.

What it does, for whom

DrugRoleForNDC
GlutamineMakes the active ingredient Emmaus Medical, Inc. 42457-420

FDA inspection history

EndedResultProgramProblems noted
Aug 11, 2023Problems found, fixed voluntarilyDrug Quality Assurance—
Dec 15, 2017Problems found, fixed voluntarilyDrug Quality Assurance—
Nov 7, 2014Problems found, fixed voluntarilyDrug Quality Assurance—

Registered with FDA for: analysis; api manufacture; label.