# Midwest Eye Laboratories Sioux Falls, LLC – FDA Inspection, Jul 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/midwest-eye-laboratories-sioux-falls-llc/f1b544b3-7f35-4bf3-bcdd-72bd539f372d
Source feed: FDA_Inspections

> FDA inspection 1211481 of Midwest Eye Laboratories Sioux Falls, LLC, July 27, 2023. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1211481
- Company Name: Midwest Eye Laboratories Sioux Falls, LLC
- Inspection Date: 2023-07-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1042349 - 2018-02-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/clifford-f-long/846e5a0c-cb7c-421c-86aa-be9fddfbaaba)

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