# FDA Inspection 1011332 - Viatek Consumer Products Group, Inc. - May 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/viatek-consumer-products-group-inc/e6c2d7d3-d9a4-4c64-9a86-ebb157da15f2
Source feed: FDA_Inspections

> FDA Inspection 1011332 for Viatek Consumer Products Group, Inc. on May 09, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1011332
- Company Name: Viatek Consumer Products Group, Inc.
- Inspection Date: 2017-05-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 563042 - 2009-01-27](https://www.keypedia.com/records/fda_inspections/viatek-consumer-products-group-inc/0d2b4a8e-b0fb-4446-ae82-f12bbf2d22ed)
- [FDA Inspection 563042 - 2009-01-27](https://www.keypedia.com/records/fda_inspections/viatek-consumer-products-group-inc/ed6a6374-62eb-49b9-8eba-d1c3981bd2a0)
- [FDA Inspection 563042 - 2009-01-27](https://www.keypedia.com/records/fda_inspections/viatek-consumer-products-group-inc/55491a58-ba27-4035-8cb6-d4da80652bf5)

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