# Distribution Inc - Inspection Records

Source: https://www.keypedia.com/companies/distribution-inc/16771853-b2cb-4e1c-b357-a8f9a77d80cc

> Inspection records and compliance data for Distribution Inc in Lincoln, Nebraska. 7 FDA inspections on record, 1 warning letter, last inspected June 29, 2026.

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## Details

- Name: Distribution Inc
- FEI Number: 3003022907
- Address Line 1: 6363 N 70th St
- City: Lincoln
- State: Nebraska
- Zip Code: 68507
- Country Name: United States
- Address: 6363 N 70th St, Lincoln, Nebraska 68507, United States
- Country: United States

## Related Documents

- [FDA Inspection 1324538 - Distribution Inc - 2026-06-29](https://www.keypedia.com/records/fda_inspections/distribution-inc/1db1e14c-f38d-4aea-bb27-3a765ef9eefb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2026
- [FDA Inspection 1313240 - Distribution Inc - 2026-04-16](https://www.keypedia.com/records/fda_inspections/distribution-inc/ce5f2527-af51-41a8-8432-63c0277027c9) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2026
- FDA Inspection 1303228 - Distribution Inc - 2026-02-23 — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2026
- FDA Inspection 1292932 - Distribution Inc - 2025-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2025
- FDA Inspection 1291470 - Distribution Inc - 2025-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2025
- [FDA Inspection 1289152 - Distribution Inc - 2025-10-29](https://www.keypedia.com/records/fda_inspections/distribution-inc/53051737-8de7-46ce-8d5e-efc567a775dd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2025
- [WARNING_LETTER - Distribution Inc - 2024-12-19](https://www.keypedia.com/records/warning_letter/distribution-inc/adbc6fff-2cfb-40be-9da3-c3e402d52ef8) — source: FDA, date: December 19, 2024
- FDA Inspection 583171 - Distribution Inc - 2009-04-07 — classification: No Action Indicated (NAI), source: FDA, date: April 7, 2009

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