# Hemagen Diagnostics Inc, Baltimore, MD – FDA Inspections

Source: https://www.keypedia.com/companies/hemagen-diagnostics-inc/ecf17e24-e402-4def-8b3a-6d7e68e19be2

> Inspection records and compliance data for Hemagen Diagnostics Inc in Baltimore, Maryland. 6 FDA inspections on record, 2 Form 483s, last inspected May 14, 2026.

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## Details

- Name: Hemagen Diagnostics Inc
- FEI Number: 1181055
- Address Line 1: 2900 Loch Raven Rd
- City: Baltimore
- State: Maryland
- Zip Code: 21218
- Country Name: United States
- Address: 2900 Loch Raven Rd, Baltimore, Maryland 21218, United States
- Country: United States

## Related Documents

- [FDA Inspection 1317040 - Hemagen Diagnostics Inc - 2026-05-14](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/93b62636-b780-4484-82a8-1062f5f511f3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2026
- FDA Inspection 1317040 - Hemagen Diagnostics Inc - 2026-05-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 14, 2026
- FDA Inspection 1208393 - Hemagen Diagnostics Inc - 2023-06-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 14, 2023
- [FDA Inspection 1037233 - Hemagen Diagnostics Inc - 2018-01-10](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/9a37d426-9ef2-4c1c-b2bf-43581dce2e7f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2018
- FDA Inspection 918077 - Hemagen Diagnostics Inc - 2015-03-10 — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2015
- FDA Inspection 918077 - Hemagen Diagnostics Inc - 2015-03-10 — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2015
- FDA Inspection 812190 - Hemagen Diagnostics Inc - 2012-12-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2012
- [FDA Inspection 812190 - Hemagen Diagnostics Inc - 2012-12-20](https://www.keypedia.com/records/fda_inspections/hemagen-diagnostics-inc/7e05ce43-8147-4113-97e7-05b629a63144) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2012
- FDA Inspection 677299 - Hemagen Diagnostics Inc - 2010-08-25 — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2010
- FDA Inspection 677299 - Hemagen Diagnostics Inc - 2010-08-25 — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2010

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