# FDA Inspection 1238825 - Gelesis Srl - February 29, 2024

Source: https://www.keypedia.com/records/fda_inspections/gelesis-srl/3051dc45-7385-48aa-ba7a-3965469100b5
Source feed: FDA_Inspections

> FDA Inspection 1238825 for Gelesis Srl on February 29, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1238825
- Company Name: Gelesis Srl
- Inspection Date: 2024-02-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/gelesis-srl/3fe4f89b-b30e-4c39-a7e4-14ebf159418b

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