# HPF S.P.A – FDA Inspection, Feb 8, 2017

Source: https://www.keypedia.com/records/fda_inspections/hpf-spa/fc4c6e16-c079-4d0d-b7e8-dcd71966c0dd
Source feed: FDA_Inspections

> FDA inspection 1003365 of HPF S.P.A, February 08, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 1003365
- Company Name: HPF S.P.A
- Inspection Date: 2017-02-08
- 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: 1

## Related Documents

- [FDA Inspection 1284260 - 2025-09-11](https://www.keypedia.com/records/fda_inspections/hpf-spa/1d1cf17e-d658-4f51-8f49-934c03b53cdd)

## Related Officers

- [Investigator](https://www.keypedia.com/people/akbar-j-zaidi/9cd9ac91-2d4b-4f6f-a975-865342075924)

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

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