# ADProducts LLC – FDA Inspection, Jun 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/adproducts-llc/3f9619bc-5807-4003-b14e-1b66525c52af
Source feed: FDA_Inspections

> FDA inspection 1015429 of ADProducts LLC, June 23, 2017. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015429
- Company Name: ADProducts LLC
- Inspection Date: 2017-06-23
- 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: 8

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/adproducts-llc/d1cf8c8d-bece-4b36-96f3-be414b49de42

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