# FDA Inspection 1210581 - Palliare, Ltd. - June 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/palliare-ltd/50eca2db-e8a8-4be0-9ac6-0adb6bc7c16d
Source feed: FDA_Inspections

> FDA Inspection 1210581 for Palliare, Ltd. on June 21, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210581
- Company Name: Palliare, Ltd.
- Inspection Date: 2023-06-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1210581 - 2023-06-21](https://www.keypedia.com/records/fda_inspections/palliare-ltd/7b18a22a-5018-40ba-8aab-b68222feed3a)

Company: https://www.keypedia.com/companies/palliare-ltd/71bf37bc-f20a-4e4f-bbd2-56f76afd34f7

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