# Octapharma Plasma, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/octapharma-plasma-inc/9287e697-2dd9-4ca0-abc6-62a8930a9be1

> Inspection records and compliance data for Octapharma Plasma, Inc. in Orange Park, Florida. Access full analysis and detailed observations.

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## Details

- Name: Octapharma Plasma, Inc.
- FEI Number: 3007302994
- City: Orange Park
- State: Florida
- Country Name: United States
- Address Line 1: 2141 Loch Rane Blvd Ste 102
- Zip Code: 32073

## Related Documents

- [FDA Inspection 1085178 - Octapharma Plasma, Inc. - 2019-03-08](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/00e5a91e-cde3-4dee-9da8-82164be7e3d3) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2019
- [FDA Inspection 999135 - Octapharma Plasma, Inc. - 2016-12-08](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/3642c6b3-b043-4232-9a22-2f8507e3425c) — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2016
- [FDA Inspection 902218 - Octapharma Plasma, Inc. - 2014-10-29](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/d08f1422-773f-46e9-8c97-8c3c8164addd) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2014
- [FDA Inspection 811207 - Octapharma Plasma, Inc. - 2012-12-13](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/0c1032e6-8ced-4eb7-bade-9daa90e41d30) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2012
- [FDA Inspection 671615 - Octapharma Plasma, Inc. - 2010-07-14](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/03b60b6a-b2d0-48fc-8e89-f8d511afcbbe) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2010
- [FDA Inspection 578896 - Octapharma Plasma, Inc. - 2009-04-29](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/37109a0d-26bb-4c5f-bdc5-a2b71ef4f062) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2009

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