# ReShape Lifesciences, Inc., Eden Prairie, MN – FDA Inspections

Source: https://www.keypedia.com/companies/reshape-lifesciences-inc/740415bf-ee64-46b0-91ff-3ff435f3769d

> Inspection records and compliance data for ReShape Lifesciences, Inc. in Eden Prairie, Minnesota. 5 FDA inspections on record, 2 Form 483s, last inspected May 22, 2019.

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## Details

- Name: ReShape Lifesciences, Inc.
- FEI Number: 3005025697
- Address Line 1: 7625 Golden Triangle Dr Ste G
- City: Eden Prairie
- State: Minnesota
- Zip Code: 55344-3700
- Country Name: United States
- Address: 7625 Golden Triangle Dr Ste G, Eden Prairie, Minnesota 55344-3700, United States
- Country: United States

## Related Documents

- [FDA Inspection 1091756 - ReShape Lifesciences, Inc. - 2019-05-22](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences-inc/e4e54b6b-de8f-410c-9f4c-67b3c01d41f9) — classification: No Action Indicated (NAI), source: FDA, date: May 22, 2019
- FDA Inspection 1091756 - ReShape Lifesciences, Inc. - 2019-05-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 22, 2019
- [FDA Inspection 1036574 - ReShape Lifesciences, Inc. - 2017-12-18](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences-inc/feb5d6d2-62f7-407c-accc-83f1f06b20bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2017
- FDA Inspection 1036574 - ReShape Lifesciences, Inc. - 2017-12-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2017
- FDA Inspection 974242 - ReShape Lifesciences, Inc. - 2016-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2016
- [FDA Inspection 856112 - ReShape Lifesciences, Inc. - 2013-11-25](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences-inc/990239b7-09ea-419b-9b89-911122298ba3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 25, 2013
- FDA Inspection 838101 - ReShape Lifesciences, Inc. - 2013-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2013

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