FDA Inspection 1271218 — Kobo Products, Inc

Kobo Products, Inc — FEI 3003926105

The FDA completed an inspection of Kobo Products, Inc on May 9, 2025 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
May 9, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Plainfield, NJ (United States)