FDA Inspection 734357 — NorMed

NorMed — FEI 3013226

The FDA completed an inspection of NorMed on June 22, 2011 in Tukwila, WA. 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
June 22, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tukwila, WA (United States)