# Insite One – FDA Inspection, Sep 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/insite-one/8e8b322d-faa7-46ba-bd3f-6b516ba480e2
Source feed: FDA_Inspections

> FDA inspection 1023771 of Insite One, September 01, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 4

## Related Documents

- [FDA Inspection 1290216 - 2025-10-31](https://www.keypedia.com/records/fda_inspections/insite-one/26de1ba5-7056-4010-a18b-4ade8a2fbc0b)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

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

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