Drug factory · FDA FEI 3007164063

Viyash Scientific Limited

UNIT-III, Survey No. 353, 354 & 467, Domadugu (Village), Gummadidala (Mandal), Sangareddy, India

India: 1

Problems found, fixed voluntarily at FDA's last inspection, Dec 6, 2024.

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

4 drug inspections on record since 2015: 0 with no problems, 4 with problems fixed voluntarily, 0 with FDA action.

What it does, for whom

DrugRoleForNDC
LinezolidMakes the active ingredient Pharmacia & Upjohn Company LLC 0009-4992

FDA inspection history

EndedResultProgramProblems noted
Dec 6, 2024Problems found, fixed voluntarilyDrug Quality Assurance—
Jul 28, 2018Problems found, fixed voluntarilyDrug Quality Assurance—
May 4, 2018Problems found, fixed voluntarilyDrug Quality Assurance—
Jun 5, 2015Problems found, fixed voluntarilyDrug Quality Assurance—

Registered with FDA for: api manufacture.