# EuroPharma, Inc., Green Bay, WI – FDA Inspections

Source: https://www.keypedia.com/companies/europharma-inc/8bc6bc28-1e3f-4abb-8f35-0d6adc44a477

> Inspection records and compliance data for EuroPharma, Inc. in Green Bay, Wisconsin. 6 FDA inspections on record (1 OAI), 1 Form 483, last inspected April 27, 2023.

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## Details

- Name: EuroPharma, Inc.
- FEI Number: 3003901837
- Address Line 1: 955 Challenger Dr
- City: Green Bay
- State: Wisconsin
- Zip Code: 54311
- Country Name: United States
- Address: 955 Challenger Dr, Green Bay, Wisconsin 54311, United States
- Country: United States

## Related Documents

- [FDA Inspection 1203907 - EuroPharma, Inc. - 2023-04-27](https://www.keypedia.com/records/fda_inspections/europharma-inc/e05a8dca-88e1-4a70-a5c0-2a081ddc728c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2023
- FDA Inspection 1203907 - EuroPharma, Inc. - 2023-04-27 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 27, 2023
- FDA Inspection 1167499 - EuroPharma, Inc. - 2022-03-10 — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2022
- FDA Inspection 1107801 - EuroPharma, Inc. - 2019-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2019
- FDA Inspection 1107801 - EuroPharma, Inc. - 2019-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2019
- FDA Inspection 974712 - EuroPharma, Inc. - 2016-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2016
- FDA Inspection 974712 - EuroPharma, Inc. - 2016-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2016
- FDA Inspection 863701 - EuroPharma, Inc. - 2014-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2014
- [FDA Inspection 769324 - EuroPharma, Inc. - 2012-02-16](https://www.keypedia.com/records/fda_inspections/europharma-inc/e9f61f38-5d23-4b51-a6bc-e33c05bd91d0) — classification: Official Action Indicated (OAI), source: FDA, date: February 16, 2012

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