# IRCA Group USA LLC - Inspection Records

Source: https://www.keypedia.com/companies/irca-group-usa-llc/9a702bd3-482b-4092-8094-8aa085af9bb5

> Inspection records and compliance data for IRCA Group USA LLC in Affton, Missouri. Access full analysis and detailed observations.

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## Details

- Name: IRCA Group USA LLC
- FEI Number: 3008627746
- City: Affton
- State: Missouri
- Country Name: United States
- Address Line 1: 8021 New Hampshire Ave
- Zip Code: 63123

## Related Documents

- [FDA Inspection 1278717 - IRCA Group USA LLC - 2025-08-11](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/4b5bc759-c233-4cdd-b1d9-bc53e8c489be) — source: FDA, date: August 11, 2025
- [FDA Inspection 1234868 - IRCA Group USA LLC - 2024-03-28](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/d643f904-7741-421f-bcc4-82716138e956) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2024
- [FDA Inspection 1172080 - IRCA Group USA LLC - 2022-04-01](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/8502e475-71e5-45f9-80f2-b4981b52fec8) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2022
- [FDA Inspection 1026930 - IRCA Group USA LLC - 2017-08-24](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/5398dd55-f6eb-4d4b-a601-3524b2bb1877) — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- [FDA Inspection 910750 - IRCA Group USA LLC - 2015-01-28](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/067a871a-8bd1-47c4-9089-602b6f525a9f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 28, 2015
- [FDA Inspection 880141 - IRCA Group USA LLC - 2014-05-23](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/833a5d79-6190-48b6-8f13-44fca1108533) — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2014
- [FDA Inspection 557410 - IRCA Group USA LLC - 2009-01-22](https://www.keypedia.com/records/fda_inspections/irca-group-usa-llc/a8e090bd-afb0-4971-9cbc-66724d773721) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2009

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