# Patheon Austria GmbH & Co. KG - Inspection Records

Source: https://www.keypedia.com/companies/patheon-austria-gmbh-co-kg/739a9a3f-4e77-4ff0-bf6e-fc2d5a48b5f3

> Inspection records and compliance data for Patheon Austria GmbH & Co. KG in Oberosterreich, 4020. Access full analysis and detailed observations.

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## Details

- Name: Patheon Austria GmbH & Co. KG
- FEI Number: 3002806853
- City: Oberosterreich
- State: 4020
- Country Name: Austria
- Address Line 1: Linz
- Zip Code: Austria
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1279175 - Patheon Austria GmbH & Co. KG - 2024-09-12](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/bf9e933e-0e7e-4b6c-846c-77fbd294662a) — source: FDA, date: September 12, 2024
- [FDA Inspection 1279175 - Patheon Austria GmbH & Co. KG - 2024-09-12](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/9724c503-ff5f-438e-a571-a0783fc5ef48) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2024
- [FDA Inspection 1098613 - Patheon Austria GmbH & Co. KG - 2018-11-30](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/d4218b03-0f66-4e70-8cd9-ca61c2817d9e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 30, 2018
- [FDA Inspection 932720 - Patheon Austria GmbH & Co. KG - 2015-05-29](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/52aee996-2dab-4e77-a147-4cb74c6a06fc) — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2015
- [FDA Inspection 794147 - Patheon Austria GmbH & Co. KG - 2012-06-01](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/ad9cd526-375e-4186-a8eb-74895129842e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2012
- [FDA Inspection 586472 - Patheon Austria GmbH & Co. KG - 2009-05-08](https://www.keypedia.com/records/fda_inspections/patheon-austria-gmbh-co-kg/77e1874c-5473-431d-803c-290f598d53c0) — classification: No Action Indicated (NAI), source: FDA, date: May 8, 2009

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