# InfoRLife SA - Inspection Records

Source: https://www.keypedia.com/companies/inforlife-sa/41fbd76a-a030-4e8b-ace1-cc13b1dc52b1

> Inspection records and compliance data for InfoRLife SA in Campascio, None. Access full analysis and detailed observations.

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## Details

- Name: InfoRLife SA
- FEI Number: 3004537783
- City: Campascio
- State: None
- Country Name: Switzerland
- Address Line 1: Casai
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - InfoRLife SA - 2024-05-03](https://www.keypedia.com/records/483/inforlife-sa/74138f7e-af41-4c36-936a-247530642eeb) — source: FDA, date: May 3, 2024
- [FDA Inspection 1239106 - InfoRLife SA - 2024-05-03](https://www.keypedia.com/records/fda_inspections/inforlife-sa/c04b82e5-e12a-421a-a655-5605d083d0da) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 3, 2024
- [FDA Inspection 1107436 - InfoRLife SA - 2019-09-10](https://www.keypedia.com/records/fda_inspections/inforlife-sa/c6492775-231b-4a43-bda8-0bde0985b4aa) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2019
- [FDA Inspection 1044861 - InfoRLife SA - 2018-02-23](https://www.keypedia.com/records/fda_inspections/inforlife-sa/8ef688ba-a155-4dde-9458-8f2a1390a79c) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2018
- [FDA Inspection 989892 - InfoRLife SA - 2016-08-16](https://www.keypedia.com/records/fda_inspections/inforlife-sa/a439bfc9-f0b4-40b8-b15d-c46c872a8a49) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2016
- [FDA Inspection 841082 - InfoRLife SA - 2013-07-04](https://www.keypedia.com/records/fda_inspections/inforlife-sa/5911d272-1022-4110-8417-08da6b52d948) — classification: No Action Indicated (NAI), source: FDA, date: July 4, 2013
- [FDA Inspection 719827 - InfoRLife SA - 2011-04-05](https://www.keypedia.com/records/fda_inspections/inforlife-sa/4564b985-2279-436a-81f2-67bca188eb63) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 5, 2011

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