# Advanced Imaging Research Inc, DBA Sree Medical Systems, Cleveland, OH – FDA Inspections

Source: https://www.keypedia.com/companies/advanced-imaging-research-inc-dba-sree-medical-systems/372add78-de80-40fb-9dc3-414ea406f9d9

> Inspection records and compliance data for Advanced Imaging Research Inc, DBA Sree Medical Systems in Cleveland, Ohio. 3 FDA inspections on record, last inspected April 11, 2018.

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## Details

- Name: Advanced Imaging Research Inc, DBA Sree Medical Systems
- FEI Number: 3004036149
- Address Line 1: 4700 Lakeside Ave E Ste 400
- City: Cleveland
- State: Ohio
- Zip Code: 44114
- Country Name: United States
- Address: 4700 Lakeside Ave E Ste 400, Cleveland, Ohio 44114, United States
- Country: United States

## Related Documents

- FDA Inspection 1049448 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2018-04-11 — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2018
- FDA Inspection 1049448 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2018-04-11 — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2018
- [FDA Inspection 755551 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2011-12-15](https://www.keypedia.com/records/fda_inspections/advanced-imaging-research-inc-dba-sree-medical-systems/a4aff5b8-7632-40e2-b3d9-ac79512303ac) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2011
- FDA Inspection 755551 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2011-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2011
- FDA Inspection 581483 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2009-06-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 2, 2009
- [FDA Inspection 581483 - Advanced Imaging Research Inc, DBA Sree Medical Systems - 2009-06-02](https://www.keypedia.com/records/fda_inspections/advanced-imaging-research-inc-dba-sree-medical-systems/c1e44c5d-18b8-41aa-9bd8-9e115cadc156) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 2, 2009

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