# FDA Inspection 803860 - Scanlan International, Inc. - October 17, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/scanlan-international-inc/e959d1e2-82ce-4dd7-88c1-ff8dd407aecb
Source feed: FDA_Inspections

> FDA Inspection 803860 for Scanlan International, Inc. on October 17, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 803860
- Company Name: Scanlan International, Inc.
- Inspection Date: 2012-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100869 - 2019-08-15](https://www.globalkeysolutions.net/records/fda_inspections/scanlan-international-inc/4ebfb5e1-b6af-42f9-af69-52175d4a4d7c)
- [FDA Inspection 1007424 - 2016-02-03](https://www.globalkeysolutions.net/records/fda_inspections/scanlan-international-inc/30634df7-53d7-4d0c-a902-3d62fe8dd662)
- [FDA Inspection 667421 - 2010-06-22](https://www.globalkeysolutions.net/records/fda_inspections/scanlan-international-inc/f8278869-d407-45c0-8a4c-c44a25ea5484)

Company: https://www.globalkeysolutions.net/companies/scanlan-international-inc/aa92ea7e-de23-46bc-8fdc-6cacefac2c83

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