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

Source: https://www.keypedia.com/records/fda_inspections/mani-inc-kiyohara-facility/9ea1d801-84a1-4d3d-b8bd-672b70dbd749
Source feed: FDA_Inspections

> FDA inspection 837793 of Mani, Inc. - Kiyohara Facility, May 23, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1060864 - 2018-07-11
- [FDA Inspection 695735 - 2010-10-07](https://www.keypedia.com/records/fda_inspections/mani-inc-kiyohara-facility/805ed79b-2d18-4bfd-a01c-71ac1b8a2832)

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

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