# Houston LDS Welfare Cannery, Houston, TX – FDA Inspections

Source: https://www.keypedia.com/companies/houston-lds-welfare-cannery/369d471a-3576-4ae6-bc1a-c3d61895088f

> Inspection records and compliance data for Houston LDS Welfare Cannery in Houston, Texas. 6 FDA inspections on record, last inspected August 15, 2025.

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## Details

- Name: Houston LDS Welfare Cannery
- FEI Number: 1000149873
- Address Line 1: 16333 Hafer Rd
- City: Houston
- State: Texas
- Zip Code: 77090
- Country Name: United States
- Address: 16333 Hafer Rd, Houston, Texas 77090, United States
- Country: United States

## Related Documents

- FDA Inspection 1278868 - Houston LDS Welfare Cannery - 2025-08-15 — source: FDA, date: August 15, 2025
- FDA Inspection 1278868 - Houston LDS Welfare Cannery - 2025-08-15 — source: FDA, date: August 15, 2025
- FDA Inspection 1278868 - Houston LDS Welfare Cannery - 2025-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2025
- FDA Inspection 1278868 - Houston LDS Welfare Cannery - 2025-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2025
- FDA Inspection 1278868 - Houston LDS Welfare Cannery - 2025-08-15 — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2025
- FDA Inspection 1026908 - Houston LDS Welfare Cannery - 2017-09-18 — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2017
- FDA Inspection 892286 - Houston LDS Welfare Cannery - 2014-08-22 — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2014
- [FDA Inspection 777395 - Houston LDS Welfare Cannery - 2012-04-12](https://www.keypedia.com/records/fda_inspections/houston-lds-welfare-cannery/449c0049-60a1-4e97-808e-e4d26ec44911) — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2012
- FDA Inspection 660405 - Houston LDS Welfare Cannery - 2010-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2010
- FDA Inspection 660405 - Houston LDS Welfare Cannery - 2010-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2010

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