# FDA Inspection 843178 - Vitalitec International, Inc. - July 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/vitalitec-international-inc/fc1da518-73cf-45c2-a62f-b94ddec7d5ce
Source feed: FDA_Inspections

> FDA Inspection 843178 for Vitalitec International, Inc. on July 19, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843178
- Company Name: Vitalitec International, Inc.
- Inspection Date: 2013-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/vitalitec-international-inc/f1d60543-23d1-4b51-bf4b-3e4356f5b370

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