# Octapharma Plasma, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/octapharma-plasma-inc/bcbc6120-e9ab-4e1d-be1f-043ce5a86851

> Inspection records and compliance data for Octapharma Plasma, Inc. in North Charleston, South Carolina. Access full analysis and detailed observations.

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## Details

- Name: Octapharma Plasma, Inc.
- FEI Number: 1076406
- City: North Charleston
- State: South Carolina
- Country Name: United States
- Address Line 1: 5900 Rivers Ave Ste F
- Zip Code: 29406

## Related Documents

- [FDA Inspection 1276299 - Octapharma Plasma, Inc. - 2025-07-09](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/2019b758-a9e7-4ab7-a62e-abbc4f8d31cd) — source: FDA, date: July 9, 2025
- [FDA Inspection 1276299 - Octapharma Plasma, Inc. - 2025-07-09](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/aeef0609-2b6d-40eb-a74e-4dcd0f1f39bf) — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2025
- [FDA Inspection 1053668 - Octapharma Plasma, Inc. - 2018-05-03](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/4924ccdc-ec49-4ea1-8fcf-6c88a396cf92) — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2018
- [FDA Inspection 930212 - Octapharma Plasma, Inc. - 2015-05-15](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/601b689c-0e42-4bff-8809-dd42963d03b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 15, 2015
- [FDA Inspection 760964 - Octapharma Plasma, Inc. - 2011-12-02](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/178ef704-a6c1-4d3a-9ebe-5f6ae2f9b9bf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 2, 2011
- [FDA Inspection 615510 - Octapharma Plasma, Inc. - 2009-09-18](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/3527a0b9-d515-43e3-8157-73bb1976e0a8) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2009

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