# Annex Medical, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/annex-medical-inc/fdb267aa-ba89-483e-a3c4-d3673014fea4

> Inspection records and compliance data for Annex Medical, Inc. in Minnetonka, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Annex Medical, Inc.
- FEI Number: 2183873
- City: Minnetonka
- State: Minnesota
- Country Name: United States
- Address Line 1: 6018 Blue Circle Dr
- Zip Code: 55343

## Related Documents

- [483 - Annex Medical, Inc. - 2023-06-09](https://www.keypedia.com/records/483/annex-medical-inc/5db4250c-ecab-4f5c-8450-41fe7f4667f7) — source: FDA, date: June 9, 2023
- [FDA Inspection 1209339 - Annex Medical, Inc. - 2023-06-09](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/e0d27abe-3c09-4620-8fb6-c13466768bb1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 9, 2023
- [FDA Inspection 1209339 - Annex Medical, Inc. - 2023-06-09](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/3a4a6136-a5d7-46c6-89b0-3ef13dfa5802) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2023
- [FDA Inspection 1108854 - Annex Medical, Inc. - 2019-10-24](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/43dffb81-912d-4cbd-9548-b25435847b27) — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2019
- [FDA Inspection 994680 - Annex Medical, Inc. - 2016-11-17](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/8db01f45-712b-4080-bb78-2f76118287f3) — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2016
- [FDA Inspection 807743 - Annex Medical, Inc. - 2012-11-05](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/2fd528c9-fe06-4020-86fd-43c45075b875) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2012
- [FDA Inspection 654345 - Annex Medical, Inc. - 2010-03-30](https://www.keypedia.com/records/fda_inspections/annex-medical-inc/dda58ce5-7827-4b25-8ca0-032fbfd506eb) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2010

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