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FDA Inspection 1129235 — Kobo Products, Inc

Kobo Products, Inc — FEI 3003926105

The FDA completed an inspection of Kobo Products, Inc on August 18, 2020 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
August 18, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Plainfield, NJ (United States)

Facility

Other inspections at this facility

  • 1271218 (VAI Fri May 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919353 (VAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919347 (VAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919349 (VAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859597 (VAI Mon Dec 16 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources