# FDA Inspection 960578 - FIMI S.r.l. - January 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/fimi-srl/d15b1111-7d4a-4000-9bde-9e332f8f8035
Source feed: FDA_Inspections

> FDA Inspection 960578 for FIMI S.r.l. on January 28, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960578
- Company Name: FIMI S.r.l.
- Inspection Date: 2016-01-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fimi-srl/af24ad0b-8147-4d8e-863b-1f4f4766dfc4

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