# Keystone Cooperative Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/keystone-cooperative-inc/50b3d2f4-668e-43d9-adf9-2b6986b7b2b5

> Inspection records and compliance data for Keystone Cooperative Inc. in Holland, Michigan. Access full analysis and detailed observations.

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## Details

- Name: Keystone Cooperative Inc.
- FEI Number: 1824467
- City: Holland
- State: Michigan
- Country Name: United States
- Address Line 1: 13400 Van Buren St
- Zip Code: 49424

## Related Documents

- [FDA Inspection 1043592 - Keystone Cooperative Inc. - 2018-02-26](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/fb8e2810-c7c5-4925-994a-c2fdf18daaa2) — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2018
- [FDA Inspection 1013453 - Keystone Cooperative Inc. - 2017-06-09](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/bcd65269-3ab0-4e5a-93a1-f4c7d3b76e1b) — classification: Official Action Indicated (OAI), source: FDA, date: June 9, 2017
- [FDA Inspection 994048 - Keystone Cooperative Inc. - 2016-12-13](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/ee5e7a36-51be-4d32-b4f3-790cc6efbecf) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2016
- [FDA Inspection 976056 - Keystone Cooperative Inc. - 2016-06-24](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/f658fe46-5a34-42d1-a68f-ab2e7567d76d) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2016
- [FDA Inspection 976251 - Keystone Cooperative Inc. - 2016-06-24](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/6695b1bb-b344-4238-a606-f9e515223ebe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2016
- [FDA Inspection 754693 - Keystone Cooperative Inc. - 2011-11-28](https://www.globalkeysolutions.net/records/fda_inspections/keystone-cooperative-inc/545cc6ae-f952-4aee-8fd3-0d4dbc07231e) — classification: No Action Indicated (NAI), source: FDA, date: November 28, 2011

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