# Octapharma Plasma, Inc., Lynchburg, VA – FDA Inspections

Source: https://www.keypedia.com/companies/octapharma-plasma-inc/3f87e0b7-6dca-4e6b-b727-0213f34cb9ac

> Inspection records and compliance data for Octapharma Plasma, Inc. in Lynchburg, Virginia. 7 FDA inspections on record, last inspected December 13, 2024.

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## Details

- Name: Octapharma Plasma, Inc.
- FEI Number: 3006295572
- Address Line 1: 6015 Fort Ave Ste 23
- City: Lynchburg
- State: Virginia
- Zip Code: 24502
- Country Name: United States
- Address: 6015 Fort Ave Ste 23, Lynchburg, Virginia 24502, United States
- Country: United States

## Related Documents

- FDA Inspection 1259244 - Octapharma Plasma, Inc. - 2024-12-13 — source: FDA, date: December 13, 2024
- FDA Inspection 1259244 - Octapharma Plasma, Inc. - 2024-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2024
- FDA Inspection 1047796 - Octapharma Plasma, Inc. - 2018-03-01 — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2018
- FDA Inspection 986379 - Octapharma Plasma, Inc. - 2016-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2016
- FDA Inspection 913736 - Octapharma Plasma, Inc. - 2015-02-10 — classification: No Action Indicated (NAI), source: FDA, date: February 10, 2015
- [FDA Inspection 897378 - Octapharma Plasma, Inc. - 2014-09-24](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/4b1c24e3-2d27-4c1c-a5e5-cd92bfa640d2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 24, 2014
- [FDA Inspection 793025 - Octapharma Plasma, Inc. - 2012-07-24](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/3a8cad01-cc76-4323-93db-4e04b2a26a1f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2012
- [FDA Inspection 638602 - Octapharma Plasma, Inc. - 2009-12-29](https://www.keypedia.com/records/fda_inspections/octapharma-plasma-inc/dea98baa-a0ed-4416-8a8d-194f43628643) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 29, 2009

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