# FDA Inspection 935561 - DNTLworks Equipment Corp. - July 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/dntlworks-equipment-corp/3dcd7f23-9404-41cd-a0d2-f03fc500020b
Source feed: FDA_Inspections

> FDA Inspection 935561 for DNTLworks Equipment Corp. on July 20, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935561
- Company Name: DNTLworks Equipment Corp.
- Inspection Date: 2015-07-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 935561 - 2015-07-20](https://www.keypedia.com/records/fda_inspections/dntlworks-equipment-corp/ba6a1995-8e27-4298-93ea-dbd8c95b279d)

Company: https://www.keypedia.com/companies/dntlworks-equipment-corp/938ff610-99e4-4dae-91fc-5033c265454a

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