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FDA Inspection 1078690 — Precision Dose Inc.

Precision Dose Inc. — FEI 1419861

The FDA completed an inspection of Precision Dose Inc. on January 28, 2019 in South Beloit, IL. 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
January 28, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
South Beloit, IL (United States)

Facility

Other inspections at this facility

  • 1281826 (VAI Thu Sep 11 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1023366 (NAI Fri May 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1000145 (NAI Fri Jan 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 748733 (NAI Mon Oct 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 723202 (NAI Mon May 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources