# Gelesis, Inc. – FDA Inspection, Jan 25, 2023

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

> FDA inspection 1195457 of Gelesis, Inc., January 25, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1076015 - 2018-12-17

## Related Officers

- [Company Rep](https://www.keypedia.com/people/james-p-finn/70e5c36c-2711-449b-bf73-e08b4dd58449)

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