# Probi USA Inc - Inspection Records

Source: https://www.keypedia.com/companies/probi-usa-inc/760a5d6a-35ca-42b0-a2ee-75061a6f2bb5

> Inspection records and compliance data for Probi USA Inc in Redmond, Washington. Access full analysis and detailed observations.

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## Details

- Name: Probi USA Inc
- FEI Number: 3004791262
- City: Redmond
- State: Washington
- Country Name: United States
- Address Line 1: 9609 153rd Ave Ne
- Zip Code: 98052

## Related Documents

- [FDA Inspection 1196727 - Probi USA Inc - 2023-02-03](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/bbd659b1-4cea-4c28-a9cb-17b200c228ed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2023
- [FDA Inspection 1196727 - Probi USA Inc - 2023-02-03](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/3d7ef2db-3e45-4cc8-846d-1289cc3e78b6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2023
- [FDA Inspection 1196727 - Probi USA Inc - 2023-02-03](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/c7756923-a7c0-4ad0-bc2d-370834d494e5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 3, 2023
- [FDA Inspection 1108388 - Probi USA Inc - 2019-09-23](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/0f833871-4725-46d0-9f1e-bc61b696b311) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2019
- [FDA Inspection 987585 - Probi USA Inc - 2016-09-28](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/d4467c3b-0182-4c4c-8fc4-7bc115c31b1d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 28, 2016
- [FDA Inspection 987585 - Probi USA Inc - 2016-09-28](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/77de5021-b03b-46a2-9007-e8b60d74042e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 28, 2016
- [FDA Inspection 987585 - Probi USA Inc - 2016-09-28](https://www.keypedia.com/records/fda_inspections/probi-usa-inc/bae12bb1-47b9-44f3-be1e-03430e83c4aa) — classification: No Action Indicated (NAI), source: FDA, date: September 28, 2016

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