# Freeman Enterprise LLC, Sturgis, MI – FDA Inspections

Source: https://www.keypedia.com/companies/freeman-enterprise-llc/177ade46-7951-4d32-9612-a29ee8b716bd

> Inspection records and compliance data for Freeman Enterprise LLC in Sturgis, Michigan. 5 FDA inspections on record, 1 Form 483, last inspected March 07, 2019.

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## Details

- Name: Freeman Enterprise LLC
- FEI Number: 1811757
- Address Line 1: 900 W Chicago Rd
- City: Sturgis
- State: Michigan
- Zip Code: 49091
- Country Name: United States
- Address: 900 W Chicago Rd, Sturgis, Michigan 49091, United States
- Country: United States

## Related Documents

- FDA Inspection 1081836 - Freeman Enterprise LLC - 2019-03-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2019
- [FDA Inspection 1081836 - Freeman Enterprise LLC - 2019-03-07](https://www.keypedia.com/records/fda_inspections/freeman-enterprise-llc/9b8c1922-d951-4916-a00d-fea7f578f1a5) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2019
- [FDA Inspection 907129 - Freeman Enterprise LLC - 2014-12-16](https://www.keypedia.com/records/fda_inspections/freeman-enterprise-llc/47371d5e-1424-4280-b487-f20ebe1cd7e4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2014
- FDA Inspection 716628 - Freeman Enterprise LLC - 2011-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2011
- FDA Inspection 716628 - Freeman Enterprise LLC - 2011-03-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 29, 2011
- FDA Inspection 668234 - Freeman Enterprise LLC - 2010-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2010
- FDA Inspection 668234 - Freeman Enterprise LLC - 2010-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2010
- FDA Inspection 611065 - Freeman Enterprise LLC - 2009-09-04 — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2009
- FDA Inspection 611065 - Freeman Enterprise LLC - 2009-09-04 — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2009

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