# Campango Limited dba Hinman Pie, Denver, CO – FDA Inspections

Source: https://www.keypedia.com/companies/campango-limited-dba-hinman-pie/9a52bec2-397b-4ec8-80c9-f5fecd8aa612

> Inspection records and compliance data for Campango Limited dba Hinman Pie in Denver, Colorado. 6 FDA inspections on record, 1 Form 483, last inspected October 30, 2024.

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## Details

- Name: Campango Limited dba Hinman Pie
- FEI Number: 3003277665
- Address Line 1: 3600 E 45th Ave
- City: Denver
- State: Colorado
- Zip Code: 80216
- Country Name: United States
- Address: 3600 E 45th Ave, Denver, Colorado 80216, United States
- Country: United States

## Related Documents

- FDA Inspection 1253445 - Campango Limited dba Hinman Pie - 2024-10-30 — source: FDA, date: October 30, 2024
- FDA Inspection 1167094 - Campango Limited dba Hinman Pie - 2022-04-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 5, 2022
- FDA Inspection 1167094 - Campango Limited dba Hinman Pie - 2022-04-05 — classification: No Action Indicated (NAI), source: FDA, date: April 5, 2022
- [FDA Inspection 1073128 - Campango Limited dba Hinman Pie - 2018-11-01](https://www.keypedia.com/records/fda_inspections/campango-limited-dba-hinman-pie/1194dad2-0249-4691-82d7-103ae600abb8) — source: FDA, date: November 1, 2018
- [FDA Inspection 987376 - Campango Limited dba Hinman Pie - 2016-07-28](https://www.keypedia.com/records/fda_inspections/campango-limited-dba-hinman-pie/76bca934-bc87-4704-894c-7ea4f1bbc7cd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2016
- [FDA Inspection 874639 - Campango Limited dba Hinman Pie - 2014-04-17](https://www.keypedia.com/records/fda_inspections/campango-limited-dba-hinman-pie/005f6097-f6bb-4395-b072-12986ef763c2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 17, 2014
- [FDA Inspection 711952 - Campango Limited dba Hinman Pie - 2011-02-25](https://www.keypedia.com/records/fda_inspections/campango-limited-dba-hinman-pie/49224d3a-771e-46a9-a1bf-054fecca26a4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 25, 2011

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