# FDA Inspection 582250 - Midwest Eye Laboratories Inc - May 11, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/midwest-eye-laboratories-inc/a45c1c98-be46-4cfc-9b19-7bcf962bf0d8
Source feed: FDA_Inspections

> FDA Inspection 582250 for Midwest Eye Laboratories Inc on May 11, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 582250
- Company Name: Midwest Eye Laboratories Inc
- Inspection Date: 2009-05-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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