# FDA Inspection 1023771 - Insite One - September 01, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/insite-one/1d6c3389-505d-499c-a5d5-53e2aa510540
Source feed: FDA_Inspections

> FDA Inspection 1023771 for Insite One on September 01, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023771
- Company Name: Insite One
- Inspection Date: 2017-09-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/insite-one/ad2c2511-9c74-4722-8aa1-632a60145a6a

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