# ImpactLife - Inspection Records

Source: https://www.globalkeysolutions.net/companies/impactlife/e53c2b86-f080-4d91-821e-1b9af0e596f1

> Inspection records and compliance data for ImpactLife in Saint Louis, Missouri. Access full analysis and detailed observations.

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## Details

- Name: ImpactLife
- FEI Number: 3005841600
- City: Saint Louis
- State: Missouri
- Country Name: United States
- Address Line 1: 9860 Watson Rd
- Zip Code: 63126

## Related Documents

- [FDA Inspection 1237165 - ImpactLife - 2024-04-24](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/5c5dd14f-5b81-4411-918e-4477e9794386) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2024
- [FDA Inspection 1069358 - ImpactLife - 2018-10-17](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/2f524e64-2e46-445c-b715-69e629609ba9) — classification: No Action Indicated (NAI), source: FDA, date: October 17, 2018
- [FDA Inspection 989407 - ImpactLife - 2016-10-18](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/b44739ce-606e-4307-9cdb-0f3f185a8d50) — classification: No Action Indicated (NAI), source: FDA, date: October 18, 2016
- [FDA Inspection 910763 - ImpactLife - 2015-01-22](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/2982a199-e575-42fd-9e7b-4b4bf35fc27e) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2015
- [FDA Inspection 821977 - ImpactLife - 2013-03-12](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/f0c719ae-a503-4823-951b-aaf9b5385ef2) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2013
- [FDA Inspection 700018 - ImpactLife - 2010-12-02](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/dde79a84-c844-46a4-8615-7ac703653553) — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2010
- [FDA Inspection 568472 - ImpactLife - 2009-02-18](https://www.globalkeysolutions.net/records/fda_inspections/impactlife/29982f2a-baef-453e-b092-a52b67e71811) — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2009

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