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FDA Inspection 1014158 — C.R. Canfield Co

C.R. Canfield Co — FEI 2127934

The FDA completed an inspection of C.R. Canfield Co on May 12, 2017 in Edina, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edina, MN (United States)

Facility

Other inspections at this facility

  • 980297 (NAI Wed Jul 27 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 898095 (NAI Mon Sep 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 678690 (NAI Wed Sep 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources