# Nenesupply Co., Ltd. – FDA Inspection, Jan 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/nenesupply-co-ltd/4ce06045-c460-4a74-9626-993691807483
Source feed: FDA_Inspections

> FDA inspection 1001748 of Nenesupply Co., Ltd., January 24, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001748
- Company Name: Nenesupply Co., Ltd.
- Inspection Date: 2017-01-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-c-mendiola/387f053a-af5f-4da9-8042-031124b9467d)

Company: https://www.keypedia.com/companies/nenesupply-co-ltd/13d23675-d18c-4b32-9dd5-c416a407b32e

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