Drug factory · FDA FEI 1931164

UnityPoint At Home

11333 Aurora Ave, Urbandale, IA, United States

United States: 1

Problems found, fixed voluntarily at FDA's last inspection, Jan 12, 2011.

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

1 drug inspection on record since 2011: 0 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.

What it does, for whom

DrugRoleForNDC
OxygenMakes it UnityPoint at Home 66698-001

FDA inspection history

EndedResultProgramProblems noted
Jan 12, 2011Problems found, fixed voluntarilyDrug Quality Assurance—

Registered with FDA for: manufacture.