# Van Elderen, Inc., Martin, MI – FDA Inspections

Source: https://www.keypedia.com/companies/van-elderen-inc/de09e695-9c6b-44e1-a316-f40ae32bcb35

> Inspection records and compliance data for Van Elderen, Inc. in Martin, Michigan. 8 FDA inspections on record, 1 Form 483, last inspected March 06, 2025.

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## Details

- Name: Van Elderen, Inc.
- FEI Number: 3002706419
- Address Line 1: 892 E Allegan St
- City: Martin
- State: Michigan
- Zip Code: 49070
- Country Name: United States
- Address: 892 E Allegan St, Martin, Michigan 49070, United States
- Country: United States

## Related Documents

- [483 - Van Elderen, Inc. - 2025-03-06](https://www.keypedia.com/records/483/van-elderen-inc/089891bf-720d-4744-bcda-e4b63ce83122) — source: FDA, date: March 6, 2025
- [FDA Inspection 1262981 - Van Elderen, Inc. - 2025-03-06](https://www.keypedia.com/records/fda_inspections/van-elderen-inc/7e224c21-543f-4a77-8d6a-32966e12f283) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2025
- FDA Inspection 1262981 - Van Elderen, Inc. - 2025-03-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2025
- FDA Inspection 994782 - Van Elderen, Inc. - 2016-12-20 — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2016
- FDA Inspection 968308 - Van Elderen, Inc. - 2016-04-28 — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2016
- FDA Inspection 906965 - Van Elderen, Inc. - 2014-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2014
- FDA Inspection 856336 - Van Elderen, Inc. - 2013-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2013
- FDA Inspection 810020 - Van Elderen, Inc. - 2012-12-07 — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2012
- FDA Inspection 750182 - Van Elderen, Inc. - 2011-10-20 — classification: No Action Indicated (NAI), source: FDA, date: October 20, 2011
- FDA Inspection 636264 - Van Elderen, Inc. - 2009-12-30 — classification: No Action Indicated (NAI), source: FDA, date: December 30, 2009

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