# Remendium Labs, LLC – FDA Inspection, Aug 3, 2016

Source: https://www.keypedia.com/records/fda_inspections/remendium-labs-llc/e81470cb-28c1-495d-8f29-8a868610eab8
Source feed: FDA_Inspections

> FDA inspection 979483 of Remendium Labs, LLC, August 03, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 979483
- Company Name: Remendium Labs, LLC
- Inspection Date: 2016-08-03
- 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: 5

Company: https://www.keypedia.com/companies/remendium-labs-llc/4274cd42-ed89-4b27-8b46-bbb9e3b6efbe

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