# Bios S.r.l. – FDA Inspection, Jul 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/bios-srl/cd5bc170-31c4-46e3-8bb7-4f6c2d8bab5f
Source feed: FDA_Inspections

> FDA inspection 1020085 of Bios S.r.l., July 13, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020085
- Company Name: Bios S.r.l.
- Inspection Date: 2017-07-13
- 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: 2

## Related Documents

- [FDA Inspection 1132100 - 2018-09-14](https://www.keypedia.com/records/fda_inspections/bios-srl/5593c7aa-cfed-4154-b33b-b08f3e6e4f5b)
- FDA Inspection 853322 - 2013-09-05

## Related Officers

- [Company Rep](https://www.keypedia.com/people/charles-l-larson/4232255d-bfd6-4616-a854-c801e4c23e1c)

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