# FDA Inspection 1257004 - Menicon America, Inc. - December 19, 2024

Source: https://www.keypedia.com/records/fda_inspections/menicon-america-inc/598d2cd5-4cdc-46bf-9da7-7360fa6b7dcd
Source feed: FDA_Inspections

> FDA Inspection 1257004 for Menicon America, Inc. on December 19, 2024. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1257004
- Company Name: Menicon America, Inc.
- Inspection Date: 2024-12-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1257004 - 2024-12-19](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/aa69839d-d9e0-4040-9f95-585f3f71e1e6)
- [FDA Inspection 1257004 - 2024-12-19](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/d799214d-dc06-48e6-8ba8-07b2239a94fe)
- [FDA Inspection 1257004 - 2024-12-19](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/5e5b657c-6578-400f-8621-82b0e13354fd)
- [FDA Inspection 1119277 - 2020-01-09](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/d80936ca-6ef9-447d-90a6-59e143f0cf9f)
- [FDA Inspection 1119277 - 2020-01-09](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/914a5068-8aa8-403a-99f8-b14a9b8f9098)

Company: https://www.keypedia.com/companies/menicon-america-inc/20fee8ca-c3a2-41e6-8111-914a6b97e48e

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