# Viatek Consumer Products Group, Inc. – FDA Inspection, Jan 27, 2009

Source: https://www.keypedia.com/records/fda_inspections/viatek-consumer-products-group-inc/ed6a6374-62eb-49b9-8eba-d1c3981bd2a0
Source feed: FDA_Inspections

> FDA inspection 563042 of Viatek Consumer Products Group, Inc., January 27, 2009. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 563042
- Company Name: Viatek Consumer Products Group, Inc.
- Inspection Date: 2009-01-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1011332 - 2017-05-09

Company: https://www.keypedia.com/companies/viatek-consumer-products-group-inc/a04c25ec-976f-4dd8-9949-d73a650447cc

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