# FDA Inspection 912665 - Weiman Products, LLC - January 29, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/weiman-products-llc/154342f8-924d-4210-9d0f-37170c676aec
Source feed: FDA_Inspections

> FDA Inspection 912665 for Weiman Products, LLC on January 29, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 912665
- Company Name: Weiman Products, LLC
- Inspection Date: 2015-01-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/weiman-products-llc/25b8a356-001c-439e-9c44-7a7013e03d0e

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