# FDA Inspection 975424 - Arciplex Llc - June 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/arciplex-llc/f4394110-927c-452c-b490-9392c0f950ae
Source feed: FDA_Inspections

> FDA Inspection 975424 for Arciplex Llc on June 28, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 975424
- Company Name: Arciplex Llc
- Inspection Date: 2016-06-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/arciplex-llc/bef14ce3-6c81-46e3-bf78-8d912eedbea0

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