# KLEB Inc, Louisville, KY – FDA Inspections

Source: https://www.keypedia.com/companies/kleb-inc/4a2a949f-8893-4a4c-afd4-87e1adea1607

> Inspection records and compliance data for KLEB Inc in Louisville, Kentucky. 7 FDA inspections on record, 1 Form 483, last inspected March 17, 2026.

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## Details

- Name: KLEB Inc
- FEI Number: 3013157033
- Address Line 1: 10160 Linn Station Rd
- City: Louisville
- State: Kentucky
- Zip Code: 40223
- Country Name: United States
- Address: 10160 Linn Station Rd, Louisville, Kentucky 40223, United States
- Country: United States

## Related Documents

- [483 - KLEB Inc - 2026-03-17](https://www.keypedia.com/records/483/kleb-inc/2eb40a22-34f3-4d71-8559-40700cbf7267) — source: FDA, date: March 17, 2026
- [FDA Inspection 1308704 - KLEB Inc - 2026-03-17](https://www.keypedia.com/records/fda_inspections/kleb-inc/e5e971ef-a499-4485-b079-21ef6776ff9d) — source: FDA, date: March 17, 2026
- FDA Inspection 1216491 - KLEB Inc - 2023-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2023
- FDA Inspection 1216491 - KLEB Inc - 2023-08-24 — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2023
- FDA Inspection 1148296 - KLEB Inc - 2021-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2021
- FDA Inspection 1148296 - KLEB Inc - 2021-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2021
- FDA Inspection 1148296 - KLEB Inc - 2021-07-28 — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2021
- FDA Inspection 1040736 - KLEB Inc - 2018-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2018
- FDA Inspection 1040736 - KLEB Inc - 2018-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2018
- FDA Inspection 957586 - KLEB Inc - 2016-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2016
- FDA Inspection 837858 - KLEB Inc - 2013-06-18 — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2013

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## Related Officers

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