# FDA Inspection 1084949 - Angelini Pharma Inc. - April 01, 2019

Source: https://www.keypedia.com/records/fda_inspections/angelini-pharma-inc/3cf27ff7-d865-4d54-a08a-97611a803783
Source feed: FDA_Inspections

> FDA Inspection 1084949 for Angelini Pharma Inc. on April 01, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084949
- Company Name: Angelini Pharma Inc.
- Inspection Date: 2019-04-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1196579 - 2022-12-06](https://www.keypedia.com/records/fda_inspections/angelini-pharma-inc/9cd961ce-9424-4472-9abb-3dda1e2b89a0)
- [FDA Inspection 1084949 - 2019-04-01](https://www.keypedia.com/records/fda_inspections/angelini-pharma-inc/0b0b4364-de5d-4cbc-a614-15aee9bc6204)

Company: https://www.keypedia.com/companies/angelini-pharma-inc/64ccb9b5-f8af-400b-a51f-715c92d3fe30

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