# Optos, PLC – FDA Inspection, Jan 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/optos-plc/c9c710e4-5bef-4c9f-b0f7-bdf5aa89c802
Source feed: FDA_Inspections

> FDA inspection 1004971 of Optos, PLC, January 26, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004971
- Company Name: Optos, PLC
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/michelle-j-glembin/e58f4652-d09f-41a7-941d-335c7b5338ad)

Company: https://www.keypedia.com/companies/optos-plc/f7a1382e-b031-417b-a11a-05bb562eedeb

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