# Missouri River Hills Elderberry Producers LLC dba River Hills Harvest, Hartsburg, MO – FDA Inspections

Source: https://www.keypedia.com/companies/missouri-river-hills-elderberry-producers-llc-dba-river-hills-harvest/a043e928-0257-4975-84f8-729853a3186e

> Inspection records and compliance data for Missouri River Hills Elderberry Producers LLC dba River Hills Harvest in Hartsburg, Missouri. 5 FDA inspections on record (1 OAI), last inspected September 24, 2026.

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## Details

- Name: Missouri River Hills Elderberry Producers LLC dba River Hills Harvest
- FEI Number: 3008720600
- Address Line 1: 19010 S Mackie Ln
- City: Hartsburg
- State: Missouri
- Zip Code: 65039
- Country Name: United States
- Address: 19010 S Mackie Ln, Hartsburg, Missouri 65039, United States
- Country: United States

## Related Documents

- FDA Inspection 1337282 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2026-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2026
- FDA Inspection 1195863 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2022-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2022
- FDA Inspection 1030397 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2017-08-14 — classification: No Action Indicated (NAI), source: FDA, date: August 14, 2017
- FDA Inspection 909786 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2014-12-30 — classification: No Action Indicated (NAI), source: FDA, date: December 30, 2014
- FDA Inspection 858720 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2014-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2014
- [FDA Inspection 858720 - Missouri River Hills Elderberry Producers LLC dba River Hills Harvest - 2014-01-24](https://www.keypedia.com/records/fda_inspections/missouri-river-hills-elderberry-producers-llc-dba-river-hills-harvest/a2f1b0e3-326e-4792-bef2-db0da2bc5c42) — classification: Official Action Indicated (OAI), source: FDA, date: January 24, 2014

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