# Wells Enterprises Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/wells-enterprises-inc/fa6d5847-d0b5-4172-b27d-caa2b987f30f

> Inspection records and compliance data for Wells Enterprises Inc in Le Mars, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Wells Enterprises Inc
- FEI Number: 1930721
- City: Le Mars
- State: Iowa
- Country Name: United States
- Address Line 1: North Ice Cream Plant, 121 2nd Ave Se
- Zip Code: 51031

## Related Documents

- [FDA Inspection 1242842 - Wells Enterprises Inc - 2024-08-16](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/f2544e5f-db15-473e-8563-e3b6c24f2ac1) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2024
- [FDA Inspection 1242844 - Wells Enterprises Inc - 2024-08-14](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/6f6248cf-5d15-462b-9c74-648e4a90e785) — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2024
- [FDA Inspection 1164679 - Wells Enterprises Inc - 2022-02-16](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/0f0ada93-07e4-430b-aaca-7de7bb97c9e1) — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2022
- [FDA Inspection 1026778 - Wells Enterprises Inc - 2017-05-24](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/d9c45b37-b865-4f82-abbe-93546cc51471) — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2017
- [FDA Inspection 965655 - Wells Enterprises Inc - 2016-03-15](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/49f7e11a-4a5f-4fcc-a7e3-94547ec11cab) — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2016
- [FDA Inspection 667099 - Wells Enterprises Inc - 2009-12-16](https://www.globalkeysolutions.net/records/fda_inspections/wells-enterprises-inc/c7299f8b-f0ed-453e-918e-deb84d7a8235) — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2009

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