# FDA Inspection 1042008 - Denovo Products LLC - February 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/denovo-products-llc/ebcfed51-1ffb-4b97-b392-75b9f5aadb43
Source feed: FDA_Inspections

> FDA Inspection 1042008 for Denovo Products LLC on February 23, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042008
- Company Name: Denovo Products LLC
- Inspection Date: 2018-02-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1042008 - 2018-02-23](https://www.keypedia.com/records/fda_inspections/denovo-products-llc/c81affb4-1708-4e0a-9685-f11f29dc5c32)

Company: https://www.keypedia.com/companies/denovo-products-llc/51434a35-c906-4fc4-be8e-4606eca7d755

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