# GE Medical Systems, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/companies/ge-medical-systems-llc/7ecbf4c0-67eb-4a30-96b8-a15e2b8cfeab

> Inspection records and compliance data for GE Medical Systems, LLC in Waukesha, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: GE Medical Systems, LLC
- FEI Number: 2183553
- City: Waukesha
- State: Wisconsin
- Country Name: United States
- Address Line 1: 3200 N Grandview Blvd
- Zip Code: 53188

## Related Documents

- [FDA Inspection 803966 - GE Medical Systems, LLC - 2012-10-11](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/6b16d158-87e1-4a81-99a0-0265946a09c9) — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2012
- [FDA Inspection 803966 - GE Medical Systems, LLC - 2012-10-11](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/cd45dc5e-884e-4d6f-8aa1-f79678882703) — classification: No Action Indicated (NAI), source: FDA, date: October 11, 2012
- [FDA Inspection 769374 - GE Medical Systems, LLC - 2012-03-02](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/aa65cd55-0779-41c6-aa6e-29a49d83229e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 2, 2012
- [FDA Inspection 769374 - GE Medical Systems, LLC - 2012-03-02](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/be6cd806-4fb6-4f6f-a459-96b9fd21b903) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 2, 2012
- [FDA Inspection 705630 - GE Medical Systems, LLC - 2011-01-11](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/7b66206f-f148-4c44-9a5e-335d48ee1e38) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 11, 2011
- [FDA Inspection 705630 - GE Medical Systems, LLC - 2011-01-11](https://www.globalkeysolutions.net/records/fda_inspections/ge-medical-systems-llc/da47f672-c0cd-4353-82ed-69dc0d71fd4c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 11, 2011

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