# FDA Inspection 1020085 - Bios S.r.l. - July 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/bios-srl/330375fc-b46b-4778-a7a2-a85f2f888b41
Source feed: FDA_Inspections

> FDA Inspection 1020085 for Bios S.r.l. on July 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020085
- Company Name: Bios S.r.l.
- Inspection Date: 2017-07-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020085 - 2017-07-13](https://www.keypedia.com/records/fda_inspections/bios-srl/cd5bc170-31c4-46e3-8bb7-4f6c2d8bab5f)
- [FDA Inspection 1020085 - 2017-07-13](https://www.keypedia.com/records/fda_inspections/bios-srl/0b25b886-61e2-42b0-9a2a-d505ede65081)
- [FDA Inspection 853322 - 2013-09-05](https://www.keypedia.com/records/fda_inspections/bios-srl/c6b3e513-ac13-497c-999b-3b530accb049)
- [FDA Inspection 853322 - 2013-09-05](https://www.keypedia.com/records/fda_inspections/bios-srl/1746a801-d0fa-421b-9094-f48690653e72)

Company: https://www.keypedia.com/companies/bios-srl/05fbda05-0c8f-4c95-8337-eea97a159348

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