# FDA Inspection 1042349 - Midwest Eye Laboratories Sioux Falls, LLC - February 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/midwest-eye-laboratories-sioux-falls-llc/d71d8e97-7388-41eb-bfdc-3b8c6736d2ae
Source feed: FDA_Inspections

> FDA Inspection 1042349 for Midwest Eye Laboratories Sioux Falls, LLC on February 15, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042349
- Company Name: Midwest Eye Laboratories Sioux Falls, LLC
- Inspection Date: 2018-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/midwest-eye-laboratories-sioux-falls-llc/3bb7cb1f-e470-4383-94f7-3fe080a8c363

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