# Octapharma Plasma, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/octapharma-plasma-inc/0ac5072d-2e4e-4a6e-844e-6a7c763152b8

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

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## Details

- Name: Octapharma Plasma, Inc.
- FEI Number: 1035346
- City: Jacksonville
- State: Florida
- Country Name: United States
- Address Line 1: 978 Arlington Rd N Ste 11
- Zip Code: 32211

## Related Documents

- [FDA Inspection 1315790 - Octapharma Plasma, Inc. - 2026-04-17](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/7b0bd622-d432-4f56-85d7-af36207fbf65) — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2026
- [FDA Inspection 1313722 - Octapharma Plasma, Inc. - 2026-04-17](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/f0fbcfdb-2232-4df9-94a3-5948269e9ba9) — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2026
- [FDA Inspection 1298618 - Octapharma Plasma, Inc. - 2026-01-09](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/5fa15954-3c72-44ce-9d15-dce51e319037) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2026
- [FDA Inspection 1255733 - Octapharma Plasma, Inc. - 2024-11-21](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/3798f79d-193b-470e-a624-30de0b5a7f15) — source: FDA, date: November 21, 2024
- [FDA Inspection 1255733 - Octapharma Plasma, Inc. - 2024-11-21](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/1eec0647-2920-4f18-82cd-53fbb1ea906a) — classification: No Action Indicated (NAI), source: FDA, date: November 21, 2024
- [FDA Inspection 1090929 - Octapharma Plasma, Inc. - 2019-04-17](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/8cc0c9a8-f2d2-414f-9ff0-20b301686539) — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2019
- [FDA Inspection 1004544 - Octapharma Plasma, Inc. - 2017-01-26](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/9366c105-dc61-45df-8892-13ad4d3bdcf4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2017
- [FDA Inspection 902074 - Octapharma Plasma, Inc. - 2014-10-29](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/6946f1be-a747-45d4-85dd-0f30033bedd6) — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2014
- [FDA Inspection 792075 - Octapharma Plasma, Inc. - 2012-07-26](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/63d183fa-a26b-4a5a-9cab-2e030edb0f06) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2012
- [FDA Inspection 767449 - Octapharma Plasma, Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/a2712f58-7543-43f5-bcaa-d0f8ab01d108) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012

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