# ImpactLife - Inspection Records

Source: https://www.globalkeysolutions.net/companies/impactlife/cf245175-7966-4f8e-9850-99d85974a419

> Inspection records and compliance data for ImpactLife in Galesburg, Illinois. Access full analysis and detailed observations.

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## Details

- Name: ImpactLife
- FEI Number: 3003319042
- City: Galesburg
- State: Illinois
- Country Name: United States
- Address Line 1: 503 Knox Square Dr Ste 107
- Zip Code: 61401

## Related Documents

- [FDA Inspection 1300408 - ImpactLife - 2026-01-28](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/ed95f458-01bd-42ca-94af-da7c24e5f301) — source: FDA, date: January 28, 2026
- [FDA Inspection 1300408 - ImpactLife - 2026-01-28](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/eb083e61-4713-4cc7-ba6b-e40b6afee701) — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2026
- [FDA Inspection 1108055 - ImpactLife - 2019-09-14](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/a750a2b7-fca1-46fe-b066-a0cd12269131) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2019
- [FDA Inspection 999366 - ImpactLife - 2017-01-23](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/2c4109ed-a3fc-4d83-821a-be5b1464e31e) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2017
- [FDA Inspection 872306 - ImpactLife - 2014-03-31](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/60cc81d8-3e57-4566-9427-8294f9aa0eb1) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2014
- [FDA Inspection 777040 - ImpactLife - 2012-04-16](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/dacaf5ce-f8d1-441c-a608-3248db0ba7b9) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2012
- [FDA Inspection 659259 - ImpactLife - 2010-04-27](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/2b007799-a913-4c7d-b877-d9e6cb1b9b71) — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2010

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