# FDA Inspection 1219110 - EYEMERA Co., Ltd. - September 07, 2023

Source: https://www.keypedia.com/records/fda_inspections/eyemera-co-ltd/e46ac933-2176-492e-869c-904fed7f6fc4
Source feed: FDA_Inspections

> FDA Inspection 1219110 for EYEMERA Co., Ltd. on September 07, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1219110
- Company Name: EYEMERA Co., Ltd.
- Inspection Date: 2023-09-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1219110 - 2023-09-07](https://www.keypedia.com/records/fda_inspections/eyemera-co-ltd/0a8b6917-aa26-480f-8cc0-da246a35bdf8)

Company: https://www.keypedia.com/companies/eyemera-co-ltd/e0f3707a-f699-47fd-9c03-97dbfde2bd13

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