# Katecho LLC - Inspection Records

Source: https://www.keypedia.com/companies/katecho-llc/11bd1e06-f3f2-490a-b3a6-0389195503d1

> Inspection records and compliance data for Katecho LLC in Des Moines, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Katecho LLC
- FEI Number: 1930027
- City: Des Moines
- State: Iowa
- Country Name: United States
- Address Line 1: 4020 Gannett Ave
- Zip Code: 50321
- Business Operations: FDF MANUFACTURE, PACK

## Related Documents

- [FDA Inspection 1229069 - Katecho LLC - 2024-08-01](https://www.keypedia.com/records/fda_inspections/katecho-llc/c284b745-0489-49f6-b3ec-604c6f486d71) — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2024
- [FDA Inspection 1229069 - Katecho LLC - 2024-08-01](https://www.keypedia.com/records/fda_inspections/katecho-llc/2ec91752-9212-4973-bc9a-e3ec7916ae1d) — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2024
- [FDA Inspection 1181164 - Katecho LLC - 2022-09-15](https://www.keypedia.com/records/fda_inspections/katecho-llc/84e2505f-3527-4a22-a8fb-876ad7decaab) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2022
- [483 - Katecho LLC - 2021-12-02](https://www.keypedia.com/records/483/katecho-llc/16098184-cdb3-4112-b5e3-cb10d3f4a531) — source: FDA, date: December 2, 2021
- [483 - Katecho LLC - 2021-07-16](https://www.keypedia.com/records/483/katecho-llc/fac9d5ad-a626-4432-9c3c-be8b3e2d7c24) — source: FDA, date: July 16, 2021
- [FDA Inspection 1147150 - Katecho LLC - 2021-07-16](https://www.keypedia.com/records/fda_inspections/katecho-llc/7ccd28a9-2e6b-4dc4-abbf-3517d01c122a) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2021
- [FDA Inspection 1147150 - Katecho LLC - 2021-07-16](https://www.keypedia.com/records/fda_inspections/katecho-llc/17e57fc5-60b9-4fd9-8688-e1975cc34da5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 16, 2021
- [FDA Inspection 1040498 - Katecho LLC - 2017-12-06](https://www.keypedia.com/records/fda_inspections/katecho-llc/c4017863-0990-4d34-b84b-fa67200d63d7) — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2017
- [FDA Inspection 1040498 - Katecho LLC - 2017-12-06](https://www.keypedia.com/records/fda_inspections/katecho-llc/4d802f2a-9982-4e22-88d3-5f998488c143) — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2017
- [FDA Inspection 1034156 - Katecho LLC - 2017-03-31](https://www.keypedia.com/records/fda_inspections/katecho-llc/da0741be-36b2-46ea-a069-bc6c2f5811a0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2017
- [FDA Inspection 1034156 - Katecho LLC - 2017-03-31](https://www.keypedia.com/records/fda_inspections/katecho-llc/79ee4155-92b1-4085-814e-624936814ad4) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2017
- [FDA Inspection 871935 - Katecho LLC - 2014-03-28](https://www.keypedia.com/records/fda_inspections/katecho-llc/c27bfe4a-c512-44a6-a6c3-f3fcab1e0a46) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2014

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