FDA Inspection 1162450 — Gulbrandsen Technologies Inc

Gulbrandsen Technologies Inc — FEI 1000111095

The FDA completed an inspection of Gulbrandsen Technologies Inc on Feb 16, 2022 in Orangeburg, SC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 16, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Orangeburg, SC (United States)