FDA Inspection
Weiman Products, LLCWeiman Products, LLC – FDA Inspection, Jan 10, 2018
Record Details
This FDA Inspection record concerns Weiman Products, LLC, with an inspection on January 10, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 56aaa746-a31c-4bba-8b0a-1a2a1baa6487
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1037374
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Weiman Products, LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 8, 2026 | Not classified | Chicago District Office | |
| January 29, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Weiman Products, LLC
- FDA Inspection 1299820 - 2026-01-08
- FDA Inspection 912665 - 2015-01-29
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