FDA Inspection 1155229 — Unither Manufacturing LLC.

Unither Manufacturing LLC. — FEI 1314625

The FDA completed an inspection of Unither Manufacturing LLC. on October 15, 2021 in Rochester, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 15, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rochester, NY (United States)