# Central Pennsylvania Blood Bank, Ephrata, PA – FDA Inspections

Source: https://www.keypedia.com/companies/central-pennsylvania-blood-bank/e65dd73b-8799-4bc0-8e12-16b5958a628e

> Inspection records and compliance data for Central Pennsylvania Blood Bank in Ephrata, Pennsylvania. 8 FDA inspections on record, last inspected March 11, 2026.

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## Details

- Name: Central Pennsylvania Blood Bank
- FEI Number: 1000161167
- Address Line 1: 446 N Reading Rd
- City: Ephrata
- State: Pennsylvania
- Zip Code: 17522
- Country Name: United States
- Address: 446 N Reading Rd, Ephrata, Pennsylvania 17522, United States
- Country: United States

## Related Documents

- FDA Inspection 1310476 - Central Pennsylvania Blood Bank - 2026-03-11 — source: FDA, date: March 11, 2026
- FDA Inspection 1310476 - Central Pennsylvania Blood Bank - 2026-03-11 — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2026
- FDA Inspection 1197535 - Central Pennsylvania Blood Bank - 2023-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2023
- FDA Inspection 1197535 - Central Pennsylvania Blood Bank - 2023-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2023
- FDA Inspection 1072439 - Central Pennsylvania Blood Bank - 2018-10-30 — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2018
- FDA Inspection 993521 - Central Pennsylvania Blood Bank - 2016-11-08 — source: FDA, date: November 8, 2016
- FDA Inspection 905793 - Central Pennsylvania Blood Bank - 2014-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2014
- FDA Inspection 817498 - Central Pennsylvania Blood Bank - 2013-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2013
- FDA Inspection 726494 - Central Pennsylvania Blood Bank - 2011-05-26 — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011
- FDA Inspection 607598 - Central Pennsylvania Blood Bank - 2009-08-26 — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2009

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