# FDA Inspection 1060864 - Mani, Inc. - Kiyohara Facility - July 11, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/7686810f-bfe8-439e-8851-459cf7c87009
Source feed: FDA_Inspections

> FDA Inspection 1060864 for Mani, Inc. - Kiyohara Facility on July 11, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060864
- Company Name: Mani, Inc. - Kiyohara Facility
- Inspection Date: 2018-07-11
- 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 1060864 - 2018-07-11](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/04b3d8a9-4863-44b1-a84b-0224780ce348)
- [FDA Inspection 837793 - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/9ea1d801-84a1-4d3d-b8bd-672b70dbd749)
- [FDA Inspection 837793 - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/64a10875-1a3a-4d4d-ae34-8538a087cfb9)
- [FDA Inspection 695735 - 2010-10-07](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/805ed79b-2d18-4bfd-a01c-71ac1b8a2832)
- [FDA Inspection 695735 - 2010-10-07](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/66fcf092-5359-4d31-892e-f4fd2e5b0de2)

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