# LAND MARK PRODUCTS  INC, Milford, IA – FDA Inspections

Source: https://www.keypedia.com/companies/land-mark-products-inc/fd53d58d-4c97-40ed-837c-e3f4b1c83cf8

> Inspection records and compliance data for LAND MARK PRODUCTS  INC in Milford, Iowa. 7 FDA inspections on record, 2 Form 483s, last inspected August 02, 2024.

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## Details

- Name: LAND MARK PRODUCTS  INC
- FEI Number: 3007324784
- Address Line 1: 2084 220th St
- City: Milford
- State: Iowa
- Zip Code: 51351
- Country Name: United States
- Address: 2084 220th St, Milford, Iowa 51351, United States
- Country: United States

## Related Documents

- FDA Inspection 1246606 - LAND MARK PRODUCTS  INC - 2024-08-02 — source: FDA, date: August 2, 2024
- FDA Inspection 1101465 - LAND MARK PRODUCTS  INC - 2019-07-24 — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2019
- [FDA Inspection 997469 - LAND MARK PRODUCTS  INC - 2016-12-16](https://www.keypedia.com/records/fda_inspections/land-mark-products-inc/45bdfbf7-6028-4715-9b13-4fceb10e38b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 16, 2016
- [FDA Inspection 994397 - LAND MARK PRODUCTS  INC - 2016-11-15](https://www.keypedia.com/records/fda_inspections/land-mark-products-inc/f498f54a-be37-4dd8-8346-752ad18c2906) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2016
- FDA Inspection 994397 - LAND MARK PRODUCTS  INC - 2016-11-15 — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2016
- FDA Inspection 968582 - LAND MARK PRODUCTS  INC - 2016-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2016
- FDA Inspection 705059 - LAND MARK PRODUCTS  INC - 2011-01-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2011
- [FDA Inspection 667039 - LAND MARK PRODUCTS  INC - 2010-05-19](https://www.keypedia.com/records/fda_inspections/land-mark-products-inc/5e9a5275-3475-4b52-8a6a-9d5aa5acbbd2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2010

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