# Biorigin,LLC - Inspection Records

Source: https://www.keypedia.com/companies/bioriginllc/df7788ec-1289-4cdf-bdaa-a66099bffe01

> Inspection records and compliance data for Biorigin,LLC in Louisville, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Biorigin,LLC
- FEI Number: 3002217540
- City: Louisville
- State: Kentucky
- Country Name: United States
- Address Line 1: 8340 Cane Run Rd
- Zip Code: 40258

## Related Documents

- [FDA Inspection 1035717 - Biorigin,LLC - 2017-11-14](https://www.keypedia.com/records/fda_inspections/bioriginllc/79f4e98b-0ac3-4926-90fc-73d5471b30e9) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2017
- [FDA Inspection 1035717 - Biorigin,LLC - 2017-11-14](https://www.keypedia.com/records/fda_inspections/bioriginllc/70b78fa6-d1db-4ed8-951e-7dfdf7989c9d) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2017
- [FDA Inspection 1035717 - Biorigin,LLC - 2017-11-14](https://www.keypedia.com/records/fda_inspections/bioriginllc/4fb1a7e9-e1b2-4a72-ac71-94b836e81813) — classification: No Action Indicated (NAI), source: FDA, date: November 14, 2017
- [FDA Inspection 934712 - Biorigin,LLC - 2015-06-03](https://www.keypedia.com/records/fda_inspections/bioriginllc/6df10df0-9b6b-497c-a2b5-4f06a1dbfc56) — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2015
- [FDA Inspection 810495 - Biorigin,LLC - 2012-12-13](https://www.keypedia.com/records/fda_inspections/bioriginllc/2047d505-fcd8-4308-9cf9-9b5b23428be8) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2012
- [FDA Inspection 602341 - Biorigin,LLC - 2009-08-06](https://www.keypedia.com/records/fda_inspections/bioriginllc/df676966-a248-4767-8be1-9e43b388147c) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2009
- [FDA Inspection 602341 - Biorigin,LLC - 2009-08-06](https://www.keypedia.com/records/fda_inspections/bioriginllc/03aa65ca-a63c-4aa9-a70a-f5926538acf9) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2009

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