# FDA Inspection 1035426 - Reshape Lifesciences - November 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/7f973476-ace2-43d1-affc-e23ffec8a510
Source feed: FDA_Inspections

> FDA Inspection 1035426 for Reshape Lifesciences on November 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035426
- Company Name: Reshape Lifesciences
- Inspection Date: 2017-11-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1041724 - 2018-02-15](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/b6a51a25-36ce-45de-a4d0-f814ea014af3)
- [FDA Inspection 1041724 - 2018-02-15](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/ea213f74-220c-4cd4-8d18-2e82ebe73e8d)
- [FDA Inspection 1035426 - 2017-11-13](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/b61be4c7-9377-4bad-a74e-cb7923b30766)
- [FDA Inspection 1035426 - 2017-11-13](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/e82f594e-fbb9-461b-990e-0e2f85b7ce10)
- [FDA Inspection 993558 - 2016-11-03](https://www.keypedia.com/records/fda_inspections/reshape-lifesciences/e4b9f1fa-27d5-4b48-a139-779eb109ecd0)

Company: https://www.keypedia.com/companies/reshape-lifesciences/f476822e-d110-4a3f-9ab4-db3ec11231f3

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