# IRCA Group USA LLC, New Century, KS – FDA Inspections

Source: https://www.keypedia.com/companies/irca-group-usa-llc/1b6b7d8b-bf2c-4e90-a17d-8396da6e8f79

> Inspection records and compliance data for IRCA Group USA LLC in New Century, Kansas. 8 FDA inspections on record, 2 Form 483s, last inspected April 26, 2024.

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## Details

- Name: IRCA Group USA LLC
- FEI Number: 1911258
- Address Line 1: 400 Prairie Village Dr
- City: New Century
- State: Kansas
- Zip Code: 66031
- Country Name: United States
- Address: 400 Prairie Village Dr, New Century, Kansas 66031, United States
- Country: United States

## Related Documents

- FDA Inspection 1237771 - IRCA Group USA LLC - 2024-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2024
- [FDA Inspection 1060053 - IRCA Group USA LLC - 2018-07-25](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/44a247f0-59b3-4a93-bb54-36054d3d6424) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 25, 2018
- [FDA Inspection 1018573 - IRCA Group USA LLC - 2017-05-19](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/14094b22-98c1-426b-9c58-e5542ab35458) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2017
- FDA Inspection 1000499 - IRCA Group USA LLC - 2017-02-16 — source: FDA, date: February 16, 2017
- [FDA Inspection 827538 - IRCA Group USA LLC - 2013-04-18](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/7c098f40-6cb5-49f4-a1f5-0f6e0a67972a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2013
- [FDA Inspection 818966 - IRCA Group USA LLC - 2013-02-14](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/925f8c2e-63dc-4c39-aa06-aeb72a8328c9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 14, 2013
- FDA Inspection 709555 - IRCA Group USA LLC - 2011-02-14 — classification: No Action Indicated (NAI), source: FDA, date: February 14, 2011
- FDA Inspection 625875 - IRCA Group USA LLC - 2009-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2009

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