# FDA Inspection 1023280 - Cadwell Industries Inc - August 16, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/cadwell-industries-inc/fcb70663-610f-4f63-ad8e-8742e79a4b5e/
Source feed: FDA_Inspections

> FDA Inspection 1023280 for Cadwell Industries Inc on August 16, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023280
- Company Name: Cadwell Industries Inc
- Inspection Date: 2017-08-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023280 - 2017-08-16](https://www.globalkeysolutions.net/api/records/fda_inspections/cadwell-industries-inc/e8184031-9d0d-4a57-b56b-3aaa54d65f46/)
- [FDA Inspection 829514 - 2013-04-30](https://www.globalkeysolutions.net/api/records/fda_inspections/cadwell-industries-inc/7cebe67d-ba11-46ad-a973-50c0237b7530/)
- [FDA Inspection 829514 - 2013-04-30](https://www.globalkeysolutions.net/api/records/fda_inspections/cadwell-industries-inc/6a5963ba-8318-42a1-9479-0fded579554c/)

Company: https://www.globalkeysolutions.net/companies/cadwell-industries-inc/56130eee-2851-42ae-bc93-fe86c6d9f38a

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