# International Marine Products Inc. Houston, Houston, TX – FDA Inspections

Source: https://www.keypedia.com/companies/international-marine-products-inc-houston/b44bc92c-8231-4364-a7f7-5fbfa2d8b124

> Inspection records and compliance data for International Marine Products Inc. Houston in Houston, Texas. 4 FDA inspections on record, 1 Form 483, last inspected March 28, 2025.

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## Details

- Name: International Marine Products Inc. Houston
- FEI Number: 3011254064
- Address Line 1: 10440 Windfern Rd Ste B
- City: Houston
- State: Texas
- Zip Code: 77064
- Country Name: United States
- Address: 10440 Windfern Rd Ste B, Houston, Texas 77064, United States
- Country: United States

## Related Documents

- FDA Inspection 1266882 - International Marine Products Inc. Houston - 2025-03-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 28, 2025
- [FDA Inspection 1266882 - International Marine Products Inc. Houston - 2025-03-28](https://www.keypedia.com/records/fda_inspections/international-marine-products-inc-houston/d8433d35-c383-4f23-82c6-dbe20d4055aa) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2025
- FDA Inspection 1266882 - International Marine Products Inc. Houston - 2025-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2025
- FDA Inspection 1146434 - International Marine Products Inc. Houston - 2021-07-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 15, 2021
- FDA Inspection 1146434 - International Marine Products Inc. Houston - 2021-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2021
- [FDA Inspection 1112173 - International Marine Products Inc. Houston - 2019-11-25](https://www.keypedia.com/records/fda_inspections/international-marine-products-inc-houston/59a27dd5-a4b6-43e1-b4bc-ff2c3847ac5b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 25, 2019
- FDA Inspection 1035048 - International Marine Products Inc. Houston - 2017-10-05 — classification: No Action Indicated (NAI), source: FDA, date: October 5, 2017

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