FDA Inspection 1083203 — K & D Laboratories Inc

K & D Laboratories Inc — FEI 3013154604

The FDA completed an inspection of K & D Laboratories Inc on March 15, 2019 in Lake Oswego, OR. 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
March 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lake Oswego, OR (United States)