# Southeastern Kentucky Rehabilitation Industries - Inspection Records

Source: https://www.keypedia.com/companies/southeastern-kentucky-rehabilitation-industries/f4570467-bc0f-4e84-a55e-f3635ca80fc9

> Inspection records and compliance data for Southeastern Kentucky Rehabilitation Industries in Corbin, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Southeastern Kentucky Rehabilitation Industries
- FEI Number: 3011390857
- City: Corbin
- State: Kentucky
- Country Name: United States
- Address Line 1: 1205 W Cumberland Gap Pkwy
- Zip Code: 40701

## Related Documents

- [FDA Inspection 1093783 - Southeastern Kentucky Rehabilitation Industries - 2019-06-11](https://www.keypedia.com/records/fda_inspections/southeastern-kentucky-rehabilitation-industries/08bff947-93ee-43b6-bd6d-802d6c23d025) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2019
- [FDA Inspection 1093783 - Southeastern Kentucky Rehabilitation Industries - 2019-06-11](https://www.keypedia.com/records/fda_inspections/southeastern-kentucky-rehabilitation-industries/ab841456-74f0-4779-a823-94271a6645db) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2019
- [FDA Inspection 998532 - Southeastern Kentucky Rehabilitation Industries - 2016-11-22](https://www.keypedia.com/records/fda_inspections/southeastern-kentucky-rehabilitation-industries/39faf5ad-1627-467a-bd53-d34b1b3fc169) — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2016
- [FDA Inspection 963933 - Southeastern Kentucky Rehabilitation Industries - 2016-03-14](https://www.keypedia.com/records/fda_inspections/southeastern-kentucky-rehabilitation-industries/b870b286-3452-446f-9f2d-e584c2ad5f8a) — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2016
- [FDA Inspection 923725 - Southeastern Kentucky Rehabilitation Industries - 2015-04-22](https://www.keypedia.com/records/fda_inspections/southeastern-kentucky-rehabilitation-industries/30c720c1-a7ff-46f6-bae2-ee8e4fe785e9) — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2015

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