# Patheon Italia S.p.A. - Inspection Records

Source: https://www.keypedia.com/companies/patheon-italia-spa/eb421078-fb58-4c48-a8ae-f1c1befb8145

> Inspection records and compliance data for Patheon Italia S.p.A. in Monza E della Brianza, 20900. Access full analysis and detailed observations.

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## Details

- Name: Patheon Italia S.p.A.
- FEI Number: 3003065803
- City: Monza E della Brianza
- State: 20900
- Country Name: Italy
- Address Line 1: Monza
- Zip Code: Italy
- Business Operations: FDF MANUFACTURE

## Related Documents

- [483 - Patheon Italia S.p.A. - Unknown Date](https://www.keypedia.com/records/483/patheon-italia-spa/6b333cf8-6726-49e5-98e0-fa970f1473f0) — source: FDA, date: Invalid Date
- [483 - Patheon Italia S.p.A. - 2023-09-29](https://www.keypedia.com/records/483/patheon-italia-spa/697016d3-1468-40c9-aab9-50d983f73540) — source: FDA, date: September 29, 2023
- [FDA Inspection 1220064 - Patheon Italia S.p.A. - 2023-09-29](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/f5f28954-b749-494d-bde5-fd872496efa9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2023
- [483 - Patheon Italia S.p.A. - 2023-09-05](https://www.keypedia.com/records/483/patheon-italia-spa/ab7e638d-4556-4e47-8f30-029b81bb0b76) — source: FDA, date: September 5, 2023
- [483 - Patheon Italia S.p.A. - 2023-05-26](https://www.keypedia.com/records/483/patheon-italia-spa/79cf157f-fd82-4b03-8b1c-6b688732e007) — source: FDA, date: May 26, 2023
- [483 - Patheon Italia S.p.A. - 2023-05-26](https://www.keypedia.com/records/483/patheon-italia-spa/f259b7b4-ddc0-4844-9cb5-7251a521313e) — source: FDA, date: May 26, 2023
- [FDA Inspection 1206297 - Patheon Italia S.p.A. - 2023-05-26](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/fed1a180-6906-49c4-8c8c-7d39fc4505b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- [FDA Inspection 1238005 - Patheon Italia S.p.A. - 2023-01-26](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/6e84e0f4-a37f-4e21-af7b-3ec8b7308634) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2023
- [483 - Patheon Italia S.p.A. - 2022-11-18](https://www.keypedia.com/records/483/patheon-italia-spa/6c026c16-362b-42d2-8eec-e7bdc8a9f447) — source: FDA, date: November 18, 2022
- [FDA Inspection 1206091 - Patheon Italia S.p.A. - 2022-04-08](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/6afa451f-d500-4cbe-ad66-d73606d7f04d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 8, 2022
- [FDA Inspection 1130741 - Patheon Italia S.p.A. - 2019-07-05](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/23d24cce-3ed3-4e5c-b530-cbfc421f2518) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 5, 2019
- [FDA Inspection 1041862 - Patheon Italia S.p.A. - 2018-02-06](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/b39a47c7-dd91-48c3-9af3-4e175dbb788c) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2018
- [FDA Inspection 977718 - Patheon Italia S.p.A. - 2016-05-20](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/2958eed5-bc4d-4630-8c5c-8e66c44c7a5c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 20, 2016
- [FDA Inspection 877083 - Patheon Italia S.p.A. - 2014-04-08](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/7e9f59f8-0ad6-4a9b-b876-b9c4649b9fe9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 8, 2014
- [FDA Inspection 839378 - Patheon Italia S.p.A. - 2013-06-11](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/7ec4e1eb-ad1f-4245-aaa9-9d7c47dd91cb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2013
- [FDA Inspection 733806 - Patheon Italia S.p.A. - 2011-06-21](https://www.keypedia.com/records/fda_inspections/patheon-italia-spa/27113431-6d42-40ac-9f53-8ad78424bd77) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2011

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