# FDA Inspection 1239139 - Perfuze LTD - May 22, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/perfuze-ltd/fde0c7a3-8ebb-4fe0-ad26-47ffcc84eeb5/
Source feed: FDA_Inspections

> FDA Inspection 1239139 for Perfuze LTD on May 22, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1239139
- Company Name: Perfuze LTD
- Inspection Date: 2024-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1239139 - 2024-05-22](https://www.globalkeysolutions.net/api/records/fda_inspections/perfuze-ltd/9bfce625-0846-4c30-98f9-6f5e08a5eef7/)

Company: https://www.globalkeysolutions.net/companies/perfuze-ltd/14af01cf-bf4e-405a-a8c0-1fe4a1c5572a

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