FDA Inspection
LOHMAN TECHNOLOGIES LLCLOHMAN TECHNOLOGIES LLC – FDA Inspection, Sep 27, 2024
Record Details
This FDA Inspection record concerns LOHMAN TECHNOLOGIES LLC, with an inspection on September 27, 2024, issued by the Minneapolis District Office, covering medical devices & rad health.
- Company
- LOHMAN TECHNOLOGIES LLC
- Inspection Date
- September 27, 2024
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · ca0299d2-1312-4469-9929-51ae47e9a1e5
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1250230
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
6- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(a)Complaints
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.22Quality Audit/Reaudit - documentation
- 21 CFR 820.40Procedures not adequately established or maintained
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Other FDA inspections of LOHMAN TECHNOLOGIES LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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