# SOFIE Co. dba SOFIE, Morgantown, WV – FDA Inspections

Source: https://www.keypedia.com/companies/sofie-co-dba-sofie/c683c431-3e42-49e6-a2fa-20743b596202

> Inspection records and compliance data for SOFIE Co. dba SOFIE in Morgantown, West Virginia. 4 FDA inspections on record, 1 Form 483, last inspected August 28, 2025.

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## Details

- Name: SOFIE Co. dba SOFIE
- FEI Number: 3005705842
- Business Operations: POSITRON EMISSION TOMOGRAPHY DRUG PRODUCTION
- Address Line 1: 64 Medical Center Dr Rm B042
- City: Morgantown
- State: West Virginia
- Zip Code: 26505
- Country Name: United States
- Address: 64 Medical Center Dr Rm B042, Morgantown, West Virginia 26505, United States
- Country: United States

## Related Documents

- [483 - SOFIE Co. dba SOFIE - 2025-10-28](https://www.keypedia.com/records/483/sofie-co-dba-sofie/bf0d4ee9-18ed-4903-b9f9-ce8931b039c5) — source: FDA, date: October 28, 2025
- [483 - SOFIE Co. dba SOFIE - 2025-08-28](https://www.keypedia.com/records/483/sofie-co-dba-sofie/374b5997-f861-441c-b979-0d0cfa5cf955) — source: FDA, date: August 28, 2025
- [FDA Inspection 1280292 - SOFIE Co. dba SOFIE - 2025-08-28](https://www.keypedia.com/records/fda_inspections/sofie-co-dba-sofie/f281f4bb-bf39-41b2-9fdc-c6b2cd5ab649) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 28, 2025
- [483 - SOFIE Co. dba SOFIE - 2022-04-21](https://www.keypedia.com/records/483/sofie-co-dba-sofie/45223af2-ae88-434e-9b7e-021fac6ff368) — source: FDA, date: April 21, 2022
- FDA Inspection 966039 - SOFIE Co. dba SOFIE - 2016-03-18 — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2016
- [FDA Inspection 882139 - SOFIE Co. dba SOFIE - 2014-06-06](https://www.keypedia.com/records/fda_inspections/sofie-co-dba-sofie/0387d49b-728d-4937-ad47-164a9a8845a6) — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2014
- [FDA Inspection 794296 - SOFIE Co. dba SOFIE - 2012-08-16](https://www.keypedia.com/records/fda_inspections/sofie-co-dba-sofie/6bd0fc2f-488a-4d55-a1b2-044ff99899e8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 16, 2012

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