# Acist Medical Systems - Inspection Records

Source: https://www.keypedia.com/companies/acist-medical-systems/0ef71d4a-1663-4fb2-b467-cab7230b02f3

> Inspection records and compliance data for Acist Medical Systems in Eden Prairie, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Acist Medical Systems
- FEI Number: 3001726808
- City: Eden Prairie
- State: Minnesota
- Country Name: United States
- Address Line 1: 7905 Fuller Rd
- Zip Code: 55344

## Related Documents

- [FDA Inspection 1166885 - Acist Medical Systems - 2022-02-28](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/e4d77c20-9c81-46ac-b24d-9c65f3d3ba8f) — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2022
- [FDA Inspection 1166885 - Acist Medical Systems - 2022-02-28](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/4d733451-f58d-49e7-aa23-44bd1412a9c7) — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2022
- [483 - Acist Medical Systems - 2019-03-04](https://www.keypedia.com/records/483/acist-medical-systems/a782bb17-f0d2-43aa-9d06-1d26b0b3a319) — source: FDA, date: March 4, 2019
- [FDA Inspection 1081356 - Acist Medical Systems - 2019-03-04](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/26fa833d-4860-48de-8b78-38ee793ae5da) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2019
- [FDA Inspection 1081356 - Acist Medical Systems - 2019-03-04](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/5deae09d-aa63-4918-92b6-f53f90cebc90) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2019
- [FDA Inspection 1081356 - Acist Medical Systems - 2019-03-04](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/7ce83345-430c-4bf9-bf10-f1f36b5c3d31) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2019
- [FDA Inspection 972358 - Acist Medical Systems - 2016-03-01](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/b3826df1-e5e6-4852-91a4-fb14fac499bf) — classification: No Action Indicated (NAI), source: FDA, date: March 1, 2016
- [FDA Inspection 783932 - Acist Medical Systems - 2012-06-06](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/9f1140d9-f37b-41d5-bc90-423d23aeeafd) — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2012
- [FDA Inspection 783932 - Acist Medical Systems - 2012-06-06](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/587e9872-12a3-46ef-9548-c11d95d5fb40) — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2012
- [FDA Inspection 654321 - Acist Medical Systems - 2010-03-24](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/ca461708-ce14-4e53-9ebe-57355f12287a) — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2010
- [FDA Inspection 654321 - Acist Medical Systems - 2010-03-24](https://www.keypedia.com/records/fda_inspections/acist-medical-systems/819db126-dd91-427d-bfa5-c472d5c0b836) — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2010

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