# FDA Inspection 837793 - Mani, Inc. - Kiyohara Facility - May 23, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/64a10875-1a3a-4d4d-ae34-8538a087cfb9
Source feed: FDA_Inspections

> FDA Inspection 837793 for Mani, Inc. - Kiyohara Facility on May 23, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 837793
- Company Name: Mani, Inc. - Kiyohara Facility
- Inspection Date: 2013-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/mani-inc-kiyohara-facility/4d67ad39-155e-479c-b7ca-05ee3901203e

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