# FDA Inspection 979483 - Remendium Labs, LLC - August 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/remendium-labs-llc/c2c056d5-6430-49e6-abae-638b5f094977
Source feed: FDA_Inspections

> FDA Inspection 979483 for Remendium Labs, LLC on August 03, 2016. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 979483 - 2016-08-03](https://www.keypedia.com/records/fda_inspections/remendium-labs-llc/e81470cb-28c1-495d-8f29-8a868610eab8)

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