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FDA Inspection 923725 — Southeastern Kentucky Rehabilitation Industries

Southeastern Kentucky Rehabilitation Industries — FEI 3011390857

The FDA completed an inspection of Southeastern Kentucky Rehabilitation Industries on April 22, 2015 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
April 22, 2015
Fiscal Year
2015
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))
  • 963933 (NAI Mon Mar 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources