# OraSure Technologies, Inc. (NASDAQ: OSUR), Bethlehem, PA – FDA Inspections

Source: https://www.keypedia.com/companies/orasure-technologies-inc/720b9d90-ff16-477c-a8a1-57eaac2aac4b

> Inspection records and compliance data for OraSure Technologies, Inc. in Bethlehem, Pennsylvania. 7 FDA inspections on record, last inspected December 13, 2018. Publicly traded as NASDAQ: OSUR.

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## Details

- Name: OraSure Technologies, Inc.
- FEI Number: 3004142665
- Address Line 1: 220 E 1st St
- City: Bethlehem
- State: Pennsylvania
- Zip Code: 18015
- Country Name: United States
- Address: 220 E 1st St, Bethlehem, Pennsylvania 18015, United States
- Country: United States

## Stock

- Stock ticker: OSUR
- Exchange: NASDAQ
- Share price: $3.38
- Market cap: $232.8M
- Price as of: November 6, 2026

## Related Documents

- FDA Inspection 1077597 - OraSure Technologies, Inc. - 2018-12-13 — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2018
- FDA Inspection 939652 - OraSure Technologies, Inc. - 2015-09-09 — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2015
- FDA Inspection 783435 - OraSure Technologies, Inc. - 2012-05-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 30, 2012
- FDA Inspection 777358 - OraSure Technologies, Inc. - 2012-04-17 — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2012
- FDA Inspection 777358 - OraSure Technologies, Inc. - 2012-04-17 — classification: No Action Indicated (NAI), source: FDA, date: April 17, 2012
- FDA Inspection 752299 - OraSure Technologies, Inc. - 2011-11-03 — classification: No Action Indicated (NAI), source: FDA, date: November 3, 2011
- FDA Inspection 653459 - OraSure Technologies, Inc. - 2010-03-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2010
- FDA Inspection 653459 - OraSure Technologies, Inc. - 2010-03-31 — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2010
- FDA Inspection 559226 - OraSure Technologies, Inc. - 2009-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2009

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