# FDA Inspection 980185 - US IOL, Inc - June 08, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/us-iol-inc/dae6aee6-eb44-4512-b45a-af02b2e58745
Source feed: FDA_Inspections

> FDA Inspection 980185 for US IOL, Inc on June 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980185
- Company Name: US IOL, Inc
- Inspection Date: 2016-06-08
- Classification: No Action Indicated (NAI)
- 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/us-iol-inc/d63f9e7f-6eb2-435d-99ef-313572e6b1dd

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