FDA Inspection 683260 — Kobo Products, Inc

Kobo Products, Inc — FEI 3003926105

The FDA completed an inspection of Kobo Products, Inc on September 30, 2010 in South Plainfield, NJ. 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
September 30, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Plainfield, NJ (United States)