Home / Inspections / 1031191

FDA Inspection 1031191 — Paradox Inc

Paradox Inc — FEI 1927976

The FDA completed an inspection of Paradox Inc on November 6, 2017 in Saint Joseph, MO. 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
November 6, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Joseph, MO (United States)

Facility

Other inspections at this facility

  • 1252435 (VAI Fri Oct 11 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1148358 (VAI Wed Aug 04 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1036549 (VAI Wed Dec 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 946214 (VAI Wed Sep 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 865872 (OAI Fri Feb 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources