# Stone Company Management, Inc., Louisville, KY – FDA Inspections

Source: https://www.keypedia.com/companies/stone-company-management-inc/f9fb8673-ec3d-431b-ad88-f1ad535323d1

> Inspection records and compliance data for Stone Company Management, Inc. in Louisville, Kentucky. 5 FDA inspections on record (1 OAI), 1 Form 483, last inspected March 07, 2017.

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## Details

- Name: Stone Company Management, Inc.
- FEI Number: 3001452084
- Address Line 1: 5700 Poplar Level Rd
- City: Louisville
- State: Kentucky
- Zip Code: 40228
- Country Name: United States
- Address: 5700 Poplar Level Rd, Louisville, Kentucky 40228, United States
- Country: United States

## Related Documents

- [FDA Inspection 1004167 - Stone Company Management, Inc. - 2017-03-07](https://www.keypedia.com/records/fda_inspections/stone-company-management-inc/73961630-6684-4b89-baf0-ffd570679dcc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2017
- FDA Inspection 897958 - Stone Company Management, Inc. - 2014-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2014
- FDA Inspection 897958 - Stone Company Management, Inc. - 2014-09-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 24, 2014
- [FDA Inspection 833159 - Stone Company Management, Inc. - 2013-05-24](https://www.keypedia.com/records/fda_inspections/stone-company-management-inc/e60e4e3c-d186-4f53-b124-43088e3e1e45) — classification: Official Action Indicated (OAI), source: FDA, date: May 24, 2013
- [FDA Inspection 816869 - Stone Company Management, Inc. - 2013-01-24](https://www.keypedia.com/records/fda_inspections/stone-company-management-inc/8134324d-c885-4d40-b4b8-4ba518a6188b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2013
- FDA Inspection 654193 - Stone Company Management, Inc. - 2010-03-11 — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2010
- FDA Inspection 654193 - Stone Company Management, Inc. - 2010-03-11 — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2010

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