FDA Inspection 1299820 — Weiman Products, LLC
The FDA completed an inspection of Weiman Products, LLC on January 8, 2026 in Gurnee, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- January 8, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gurnee, IL (United States)