# FDA Inspection 1037308 - Midwest Eye Laboratories Woodbury, LLC - January 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/midwest-eye-laboratories-woodbury-llc/fceca7e0-8abb-4ffc-9924-4f34d24f6622/
Source feed: FDA_Inspections

> FDA Inspection 1037308 for Midwest Eye Laboratories Woodbury, LLC on January 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037308
- Company Name: Midwest Eye Laboratories Woodbury, LLC
- Inspection Date: 2018-01-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 914188 - 2015-02-13](https://www.globalkeysolutions.net/api/records/fda_inspections/midwest-eye-laboratories-woodbury-llc/a36adcf5-a69a-405e-9add-fea3106efeef/)
- [FDA Inspection 774767 - 2012-03-27](https://www.globalkeysolutions.net/api/records/fda_inspections/midwest-eye-laboratories-woodbury-llc/c0824edf-eaec-454d-8dd2-62a8a639a4f0/)

Company: https://www.globalkeysolutions.net/companies/midwest-eye-laboratories-woodbury-llc/a164b00b-020e-4d9e-8b12-0a8cbba4a4d3

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