# FDA Inspection 1284260 - HPF S.P.A - September 11, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/hpf-spa/d6c7e272-1a0f-4c90-9d2b-a45e3cf980b4
Source feed: FDA_Inspections

> FDA Inspection 1284260 for HPF S.P.A on September 11, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1284260
- Company Name: HPF S.P.A
- Inspection Date: 2025-09-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1284260 - 2025-09-11](https://www.globalkeysolutions.net/records/fda_inspections/hpf-spa/1d1cf17e-d658-4f51-8f49-934c03b53cdd)
- [FDA Inspection 1284260 - 2025-09-11](https://www.globalkeysolutions.net/records/fda_inspections/hpf-spa/c679eef3-48eb-431e-9acc-9c34e8cb75f9)
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- [FDA Inspection 1003365 - 2017-02-08](https://www.globalkeysolutions.net/records/fda_inspections/hpf-spa/fc4c6e16-c079-4d0d-b7e8-dcd71966c0dd)

Company: https://www.globalkeysolutions.net/companies/hpf-spa/32ef27c4-dfab-4a8b-9910-c4f180952d8e

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