# BPC Plasma, Inc., Dickson City, PA – FDA Inspections

Source: https://www.keypedia.com/companies/bpc-plasma-inc/30b34edd-f21a-42fd-9f57-732e71cd75dc

> Inspection records and compliance data for BPC Plasma, Inc. in Dickson City, Pennsylvania. 9 FDA inspections on record, last inspected December 05, 2025.

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## Details

- Name: BPC Plasma, Inc.
- FEI Number: 2572436
- Address Line 1: 1027 Commerce Blvd
- City: Dickson City
- State: Pennsylvania
- Zip Code: 18519
- Country Name: United States
- Address: 1027 Commerce Blvd, Dickson City, Pennsylvania 18519, United States
- Country: United States

## Related Documents

- [FDA Inspection 1294756 - BPC Plasma, Inc. - 2025-12-05](https://www.keypedia.com/records/fda_inspections/bpc-plasma-inc/caa5314c-0d48-4451-8104-b10b10e844c4) — source: FDA, date: December 5, 2025
- FDA Inspection 1294756 - BPC Plasma, Inc. - 2025-12-05 — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2025
- [FDA Inspection 1147613 - BPC Plasma, Inc. - 2021-07-19](https://www.keypedia.com/records/fda_inspections/bpc-plasma-inc/6f014d16-0351-4593-af1b-e704ac9b580e) — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2021
- FDA Inspection 1147613 - BPC Plasma, Inc. - 2021-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2021
- FDA Inspection 1057146 - BPC Plasma, Inc. - 2018-06-14 — classification: No Action Indicated (NAI), source: FDA, date: June 14, 2018
- FDA Inspection 971876 - BPC Plasma, Inc. - 2016-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2016
- FDA Inspection 881184 - BPC Plasma, Inc. - 2014-05-30 — classification: No Action Indicated (NAI), source: FDA, date: May 30, 2014
- FDA Inspection 805482 - BPC Plasma, Inc. - 2012-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2012
- FDA Inspection 788845 - BPC Plasma, Inc. - 2012-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2012
- FDA Inspection 677539 - BPC Plasma, Inc. - 2010-08-25 — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2010

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