# Octapharma Plasma, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/octapharma-plasma-inc/28a5aba6-53fa-4df4-bb2c-8405d9dcc45e

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

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## Details

- Name: Octapharma Plasma, Inc.
- FEI Number: 3007320762
- City: Spokane
- State: Washington
- Country Name: United States
- Address Line 1: 510 E Francis Ave
- Zip Code: 99208

## Related Documents

- [FDA Inspection 1063372 - Octapharma Plasma, Inc. - 2018-07-26](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/db0b2e48-8b7a-4c11-bb8d-94afaddfed4e) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2018
- [FDA Inspection 961928 - Octapharma Plasma, Inc. - 2016-03-01](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/99a82a8e-3bf7-4529-8dc3-925534867bbd) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2016
- [FDA Inspection 863455 - Octapharma Plasma, Inc. - 2014-01-17](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/be3bb163-a9bf-4360-9b55-a29b11b0b4f9) — classification: No Action Indicated (NAI), source: FDA, date: January 17, 2014
- [FDA Inspection 775893 - Octapharma Plasma, Inc. - 2012-02-29](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/fe7666c8-ae71-485c-99e1-da9a9ba6b944) — classification: No Action Indicated (NAI), source: FDA, date: February 29, 2012
- [FDA Inspection 648308 - Octapharma Plasma, Inc. - 2010-02-24](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/dd3527c3-68cc-4c13-a762-a02ead13277e) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2010
- [FDA Inspection 603088 - Octapharma Plasma, Inc. - 2009-07-01](https://www.globalkeysolutions.net/records/fda_inspections/octapharma-plasma-inc/bb587ea1-4182-4712-900e-0c81a9a0d16c) — classification: No Action Indicated (NAI), source: FDA, date: July 1, 2009

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