# Sauer Brands, Inc., Mauldin, SC – FDA Inspections

Source: https://www.keypedia.com/companies/sauer-brands-inc/81862bb2-f9b1-4014-865a-7531ef572877

> Inspection records and compliance data for Sauer Brands, Inc. in Mauldin, South Carolina. 6 FDA inspections on record, last inspected March 07, 2025.

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## Details

- Name: Sauer Brands, Inc.
- FEI Number: 1012980
- Address Line 1: 728 N Main St
- City: Mauldin
- State: South Carolina
- Zip Code: 29662
- Country Name: United States
- Address: 728 N Main St, Mauldin, South Carolina 29662, United States
- Country: United States

## Related Documents

- [FDA Inspection 1229982 - Sauer Brands, Inc. - 2025-03-07](https://www.keypedia.com/records/fda_inspections/sauer-brands-inc/cedcbdd1-015e-4ca5-9f88-91669a1e1657) — source: FDA, date: March 7, 2025
- FDA Inspection 1229982 - Sauer Brands, Inc. - 2025-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2025
- FDA Inspection 1229982 - Sauer Brands, Inc. - 2025-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1153366 - Sauer Brands, Inc. - 2021-09-30](https://www.keypedia.com/records/fda_inspections/sauer-brands-inc/b6c8fe1f-b576-4d06-9359-8771f2ed861a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2021
- FDA Inspection 1056553 - Sauer Brands, Inc. - 2018-06-22 — source: FDA, date: June 22, 2018
- FDA Inspection 1054428 - Sauer Brands, Inc. - 2018-02-14 — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2018
- FDA Inspection 872702 - Sauer Brands, Inc. - 2014-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2014
- FDA Inspection 655760 - Sauer Brands, Inc. - 2010-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2010
- FDA Inspection 655760 - Sauer Brands, Inc. - 2010-03-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2010
- FDA Inspection 655760 - Sauer Brands, Inc. - 2010-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2010

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