# Patheon Softgels Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/patheon-softgels-inc/10cb6876-0398-4373-a33a-1d1e4c2bcf82

> Inspection records and compliance data for Patheon Softgels Inc. in High Point, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: Patheon Softgels Inc.
- FEI Number: 3001451366
- City: High Point
- State: North Carolina
- Country Name: United States
- Address Line 1: 4125 Premier Dr
- Zip Code: 27265
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - Patheon Softgels Inc. - 2025-07-17](https://www.globalkeysolutions.net/records/483/patheon-softgels-inc/4f88737c-2d35-45cb-8564-ff4184f245b2) — source: FDA, date: July 17, 2025
- [FDA Inspection 1251557 - Patheon Softgels Inc. - 2025-07-17](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/90bbc81f-a1fc-4744-9950-69d407beb2a8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2025
- [FDA Inspection 1080798 - Patheon Softgels Inc. - 2019-01-30](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/7d15b8cd-5597-4a83-adf4-0ebe8dc4994c) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2019
- [FDA Inspection 1023652 - Patheon Softgels Inc. - 2017-08-11](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/b8cdb143-dc59-4867-8c59-399a58e1d4bf) — classification: No Action Indicated (NAI), source: FDA, date: August 11, 2017
- [FDA Inspection 912784 - Patheon Softgels Inc. - 2015-01-29](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/d75b5386-787e-40c8-be5b-21f6d7f2cbea) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2015
- [FDA Inspection 852044 - Patheon Softgels Inc. - 2013-09-18](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/2c17a97d-0102-4392-a23e-4bf26ab5c07d) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2013
- [FDA Inspection 801960 - Patheon Softgels Inc. - 2012-09-26](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/b5ed995f-dc33-4e1c-bb1f-98fcaf3fc794) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2012
- [FDA Inspection 789295 - Patheon Softgels Inc. - 2012-07-02](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/fbc7d929-77c4-4730-a408-ac5407151340) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2012
- [FDA Inspection 785441 - Patheon Softgels Inc. - 2012-06-06](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/38509d60-750e-4f3a-b1f5-2faedf07ddb8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 6, 2012
- [FDA Inspection 684621 - Patheon Softgels Inc. - 2010-09-14](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/789f9ae2-f997-4efa-87e9-993921ad2858) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2010
- [FDA Inspection 612191 - Patheon Softgels Inc. - 2009-09-21](https://www.globalkeysolutions.net/records/fda_inspections/patheon-softgels-inc/ef7a53e2-4144-4778-86a8-f7918772544d) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2009

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