# FDA Inspection 1042437 - Direct Crown Products, LLC - February 27, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/direct-crown-products-llc/41c3493b-e231-4076-ad20-1e930626f309
Source feed: FDA_Inspections

> FDA Inspection 1042437 for Direct Crown Products, LLC on February 27, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042437
- Company Name: Direct Crown Products, LLC
- Inspection Date: 2018-02-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1042437 - 2018-02-27](https://www.globalkeysolutions.net/records/fda_inspections/direct-crown-products-llc/c7a432b3-f8d4-4c61-a07e-9b19ed917940)

Company: https://www.globalkeysolutions.net/companies/direct-crown-products-llc/9b3fbb7b-aa4e-4715-aa24-da2b23506271

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