# FDA Inspection 1211481 - Midwest Eye Laboratories Sioux Falls, LLC - July 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 for Midwest Eye Laboratories Sioux Falls, LLC on July 27, 2023. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1211481 - 2023-07-27](https://www.keypedia.com/records/fda_inspections/midwest-eye-laboratories-sioux-falls-llc/b61ea48a-ace9-4dd3-9daa-0682e197e551)
- [FDA Inspection 1042349 - 2018-02-15](https://www.keypedia.com/records/fda_inspections/midwest-eye-laboratories-sioux-falls-llc/d71d8e97-7388-41eb-bfdc-3b8c6736d2ae)

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