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FDA Inspection 803860 — Scanlan International, Inc.

Scanlan International, Inc. — FEI 2126670

The FDA completed an inspection of Scanlan International, Inc. on October 17, 2012 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 17, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1100869 (NAI Thu Aug 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007424 (NAI Wed Feb 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 667421 (NAI Tue Jun 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources