# FDA Inspection 999090 - Orvim SRL - January 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/orvim-srl/e5db2c17-d40d-4ada-909a-5e19140035bc
Source feed: FDA_Inspections

> FDA Inspection 999090 for Orvim SRL on January 24, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 999090
- Company Name: Orvim SRL
- Inspection Date: 2017-01-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/orvim-srl/7f79f71a-0128-4c29-8d4a-4f0336c740fb

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