# FDA Inspection 1195457 - Gelesis, Inc. - January 25, 2023

Source: https://www.keypedia.com/records/fda_inspections/gelesis-inc/f3bc2214-2ff6-424c-801e-fec998b04eb8
Source feed: FDA_Inspections

> FDA Inspection 1195457 for Gelesis, Inc. on January 25, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195457
- Company Name: Gelesis, Inc.
- Inspection Date: 2023-01-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1195457 - 2023-01-25](https://www.keypedia.com/records/fda_inspections/gelesis-inc/8768054e-a87a-4eb0-b4fe-9ec504ca9056)
- [FDA Inspection 1076015 - 2018-12-17](https://www.keypedia.com/records/fda_inspections/gelesis-inc/3e1c39ab-dd5b-48cc-b28f-7da150f40ab9)

Company: https://www.keypedia.com/companies/gelesis-inc/ab1dbf70-1fab-4584-81fd-7ff5de4fa712

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