# FDA Inspection 695735 - Mani, Inc. - Kiyohara Facility - October 07, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/805ed79b-2d18-4bfd-a01c-71ac1b8a2832
Source feed: FDA_Inspections

> FDA Inspection 695735 for Mani, Inc. - Kiyohara Facility on October 07, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695735
- Company Name: Mani, Inc. - Kiyohara Facility
- Inspection Date: 2010-10-07
- 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.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