Drug factory · FDA FEI 3002807989

Recordati Industria Chimica E Farmaceutica SpA

Via Mediana Cisterna 4, Campoverde di Aprilia (Latina), Italy

Italy: 1

Problems found, fixed voluntarily at FDA's last inspection, Oct 3, 2025.

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

6 drug inspections on record since 2010: 1 with no problems, 5 with problems fixed voluntarily, 0 with FDA action.

What it does, for whom

DrugRoleForNDC
AcyclovirMakes the active ingredient Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 23155-227, 23155-228

FDA inspection history

EndedResultProgramProblems noted
Oct 3, 2025Problems found, fixed voluntarilyDrug Quality Assurance—
Sep 30, 2022Problems found, fixed voluntarilyDrug Quality Assurance—
Jun 22, 2019Problems found, fixed voluntarilyDrug Quality Assurance—
Jun 7, 2018No problems foundDrug Quality Assurance—
Jul 1, 2016Problems found, fixed voluntarilyDrug Quality Assurance—
Jul 23, 2010Problems found, fixed voluntarilyDrug Quality Assurance—

Registered with FDA for: api manufacture; manufacture.