# Terumo Medical Corporation, Elkton, MD – FDA Inspections

Source: https://www.keypedia.com/companies/terumo-medical-corporation/436e47e6-b836-4f48-9dbf-0a2f76c31902

> Inspection records and compliance data for Terumo Medical Corporation in Elkton, Maryland. 9 FDA inspections on record (1 OAI), 3 Form 483s, last inspected September 11, 2026.

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## Details

- Name: Terumo Medical Corporation
- FEI Number: 1118880
- Address Line 1: 950 Elkton Blvd
- City: Elkton
- State: Maryland
- Zip Code: 21921
- Country Name: United States
- Address: 950 Elkton Blvd, Elkton, Maryland 21921, United States
- Country: United States

## Related Documents

- [FDA Inspection 1332082 - Terumo Medical Corporation - 2026-09-11](https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/bb0841ec-3486-4120-bce6-9be752b33b50) — source: FDA, date: September 11, 2026
- FDA Inspection 1317212 - Terumo Medical Corporation - 2026-05-01 — source: FDA, date: May 1, 2026
- [483 - Terumo Medical Corporation - 2022-10-28](https://www.keypedia.com/records/483/terumo-medical-corporation/f462bd5d-fd61-4d02-ae1b-c50b0354f2a1) — source: FDA, date: October 28, 2022
- FDA Inspection 1182280 - Terumo Medical Corporation - 2022-10-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 28, 2022
- FDA Inspection 1182280 - Terumo Medical Corporation - 2022-10-28 — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2022
- [483 - Terumo Medical Corporation - 2019-06-20](https://www.keypedia.com/records/483/terumo-medical-corporation/79a2c9f1-4910-49c9-8a36-209ea035e676) — source: FDA, date: June 20, 2019
- [FDA Inspection 1094113 - Terumo Medical Corporation - 2019-06-20](https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/64690c93-12b4-40b1-833d-882ddc9f0d1b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2019
- FDA Inspection 1003680 - Terumo Medical Corporation - 2017-01-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2017
- [FDA Inspection 1003680 - Terumo Medical Corporation - 2017-01-13](https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/9a2c1384-ab67-43d2-8e01-8c3414dafafd) — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2017
- [FDA Inspection 950051 - Terumo Medical Corporation - 2015-10-23](https://www.keypedia.com/records/fda_inspections/terumo-medical-corporation/4d393933-8ed0-49ba-903e-7a39b5ada30e) — classification: Official Action Indicated (OAI), source: FDA, date: October 23, 2015
- FDA Inspection 847650 - Terumo Medical Corporation - 2013-09-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2013
- FDA Inspection 847650 - Terumo Medical Corporation - 2013-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013

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## Related Officers

- [Jacob M Dyer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)
- [investigator](https://www.keypedia.com/people/daniel-t-lee/8147e5b2-2065-42e3-b86c-36c0231f74cc)
- [Lindsey L Kirsh](https://www.keypedia.com/people/lindsey-l-kirsh/78c606cb-8c62-4b99-9e71-56ab53ed2a3c)
- [Jude C. Dike](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)