# FDA Inspection 1036574 - ReShape Lifesciences, Inc. - December 18, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/reshape-lifesciences-inc/feb5d6d2-62f7-407c-accc-83f1f06b20bc/
Source feed: FDA_Inspections

> FDA Inspection 1036574 for ReShape Lifesciences, Inc. on December 18, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1036574
- Company Name: ReShape Lifesciences, Inc.
- Inspection Date: 2017-12-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/reshape-lifesciences-inc/740415bf-ee64-46b0-91ff-3ff435f3769d

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7