# Capriole, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/capriole-inc/1d69c120-401d-41be-8d64-b7d9a4564be0

> Inspection records and compliance data for Capriole, Inc. in Greenville, Indiana. Access full analysis and detailed observations.

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## Details

- Name: Capriole, Inc.
- FEI Number: 1000143469
- City: Greenville
- State: Indiana
- Country Name: United States
- Address Line 1: 10329 New Cut Rd
- Zip Code: 47124

## Related Documents

- [FDA Inspection 1208064 - Capriole, Inc. - 2023-06-07](https://www.keypedia.com/records/fda_inspections/capriole-inc/2dba2d1a-24eb-40e8-874a-40cbab588660) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2023
- [FDA Inspection 1177351 - Capriole, Inc. - 2022-08-11](https://www.keypedia.com/records/fda_inspections/capriole-inc/64cdb92b-9900-4b51-95f8-300c72d1746d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2022
- [FDA Inspection 1177351 - Capriole, Inc. - 2022-08-11](https://www.keypedia.com/records/fda_inspections/capriole-inc/96973ca0-fae4-4ca9-8f42-dc3d7bb175ee) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2022
- [FDA Inspection 1103031 - Capriole, Inc. - 2019-07-02](https://www.keypedia.com/records/fda_inspections/capriole-inc/dcaca6ed-6afc-4241-a31e-a06f50251ccc) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2019
- [FDA Inspection 977008 - Capriole, Inc. - 2016-07-11](https://www.keypedia.com/records/fda_inspections/capriole-inc/b93950cf-2053-4640-9208-9edd29570711) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2016
- [FDA Inspection 759856 - Capriole, Inc. - 2011-12-21](https://www.keypedia.com/records/fda_inspections/capriole-inc/349b96e4-00a6-46ec-813c-37c3f56d70da) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2011
- [FDA Inspection 759856 - Capriole, Inc. - 2011-12-21](https://www.keypedia.com/records/fda_inspections/capriole-inc/0390bff3-7d1a-4248-a5fa-78d18b85fb93) — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2011

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