# Weiman Products, LLC – FDA Inspection, Jan 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/weiman-products-llc/56aaa746-a31c-4bba-8b0a-1a2a1baa6487
Source feed: FDA_Inspections

> FDA inspection 1037374 of Weiman Products, LLC, January 10, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037374
- Company Name: Weiman Products, LLC
- Inspection Date: 2018-01-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1299820 - 2026-01-08
- FDA Inspection 912665 - 2015-01-29

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-z-lu/17448aca-e316-424c-b7b2-88c8baffc359)

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

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