# A. L. Schutzman Company, Inc., Waukesha, WI – FDA Inspections

Source: https://www.keypedia.com/companies/a-l-schutzman-company-inc/9c50ddc4-9aa2-4691-b758-97a12ce4fefb

> Inspection records and compliance data for A. L. Schutzman Company, Inc. in Waukesha, Wisconsin. 15 FDA inspections on record, 1 Form 483, last inspected January 06, 2026.

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## Details

- Name: A. L. Schutzman Company, Inc.
- FEI Number: 2121093
- Address Line 1: N21w23560 Ridgeview Pkwy W
- City: Waukesha
- State: Wisconsin
- Zip Code: 53188
- Country Name: United States
- Address: N21w23560 Ridgeview Pkwy W, Waukesha, Wisconsin 53188, United States
- Country: United States

## Related Documents

- FDA Inspection 1298414 - A. L. Schutzman Company, Inc. - 2026-01-06 — source: FDA, date: January 6, 2026
- FDA Inspection 1298414 - A. L. Schutzman Company, Inc. - 2026-01-06 — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2026
- FDA Inspection 1238447 - A. L. Schutzman Company, Inc. - 2024-05-07 — source: FDA, date: May 7, 2024
- FDA Inspection 1156376 - A. L. Schutzman Company, Inc. - 2021-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2021
- FDA Inspection 1075834 - A. L. Schutzman Company, Inc. - 2019-01-02 — source: FDA, date: January 2, 2019
- FDA Inspection 1075842 - A. L. Schutzman Company, Inc. - 2018-11-19 — source: FDA, date: November 19, 2018
- [FDA Inspection 1027771 - A. L. Schutzman Company, Inc. - 2017-10-03](https://www.keypedia.com/records/fda_inspections/a-l-schutzman-company-inc/5aea2ad0-5608-4b46-a9cc-14666dd247ba) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 3, 2017
- FDA Inspection 952577 - A. L. Schutzman Company, Inc. - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 952577 - A. L. Schutzman Company, Inc. - 2015-11-24 — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2015
- FDA Inspection 855792 - A. L. Schutzman Company, Inc. - 2013-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2013

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