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

Source: https://www.keypedia.com/records/fda_inspections/menicon-america-inc/aa69839d-d9e0-4040-9f95-585f3f71e1e6
Source feed: FDA_Inspections

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

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## 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: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1257004 - 2024-12-19](https://www.keypedia.com/records/fda_inspections/menicon-america-inc/d799214d-dc06-48e6-8ba8-07b2239a94fe)
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Company: https://www.keypedia.com/companies/menicon-america-inc/20fee8ca-c3a2-41e6-8111-914a6b97e48e

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144