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FDA Inspection 963933 — Southeastern Kentucky Rehabilitation Industries

Southeastern Kentucky Rehabilitation Industries — FEI 3011390857

The FDA completed an inspection of Southeastern Kentucky Rehabilitation Industries on March 14, 2016 in Corbin, KY. 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
March 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Corbin, KY (United States)

Facility

Other inspections at this facility

  • 1093783 (NAI Tue Jun 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998532 (NAI Tue Nov 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923725 (NAI Wed Apr 22 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources