# Mani, Inc. - Kiyohara Facility - Inspection Records

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

> Inspection records and compliance data for Mani, Inc. - Kiyohara Facility in Utsunomiya, None. Access full analysis and detailed observations.

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## Details

- Name: Mani, Inc. - Kiyohara Facility
- FEI Number: 3002692886
- City: Utsunomiya
- State: None
- Country Name: Japan
- Address Line 1: Park 8-3, Kiyoharakogyodanchi;  Kiyoharakogyodanchi; Kiyoharakogyodanchi
- Zip Code: None

## Related Documents

- [FDA Inspection 1060864 - Mani, Inc. - Kiyohara Facility - 2018-07-11](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/04b3d8a9-4863-44b1-a84b-0224780ce348) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2018
- [FDA Inspection 1060864 - Mani, Inc. - Kiyohara Facility - 2018-07-11](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/7686810f-bfe8-439e-8851-459cf7c87009) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2018
- [FDA Inspection 837793 - Mani, Inc. - Kiyohara Facility - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/9ea1d801-84a1-4d3d-b8bd-672b70dbd749) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2013
- [FDA Inspection 837793 - Mani, Inc. - Kiyohara Facility - 2013-05-23](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/64a10875-1a3a-4d4d-ae34-8538a087cfb9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2013
- [FDA Inspection 695735 - Mani, Inc. - Kiyohara Facility - 2010-10-07](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/805ed79b-2d18-4bfd-a01c-71ac1b8a2832) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 7, 2010
- [FDA Inspection 695735 - Mani, Inc. - Kiyohara Facility - 2010-10-07](https://www.globalkeysolutions.net/records/fda_inspections/mani-inc-kiyohara-facility/66fcf092-5359-4d31-892e-f4fd2e5b0de2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 7, 2010

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