# FDA Inspection 945317 - Menicon America, Inc. - August 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/menicon-america-inc/04db3900-2e62-486f-85dd-9b8cec9876be
Source feed: FDA_Inspections

> FDA Inspection 945317 for Menicon America, Inc. on August 26, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 945317
- Company Name: Menicon America, Inc.
- Inspection Date: 2015-08-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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