FEI 3012267350
Lohman Technologies, Llc
N27W23953 Paul Rd Ste 204, Pewaukee, WI, US
MDR events21All time
Recalls0All time
Registered products1
Establishment typeManufactureManufacture Medical Device
Registered product codes
1 product codes
Recent MDR events
21 on file
- HOMECG+Dec 12, 2025Malfunction3012267350-2025-00019
- HOMECG+Dec 12, 2025Malfunction3012267350-2025-00020
- HOMECG+Dec 12, 2025Malfunction3012267350-2025-00017
- HOMECG+Dec 12, 2025Malfunction3012267350-2025-00018
- HOMECGDec 12, 2025Malfunction3012267350-2025-00016
- HOMECG+Dec 12, 2025Malfunction3012267350-2025-00021
- HOMECG+Oct 30, 2025Malfunction3012267350-2025-00015
- HOMECG+Sep 12, 2025Malfunction3012267350-2025-00014
- HOMECG+Sep 12, 2025Malfunction3012267350-2025-00013
- HOMECG+Aug 22, 2025Malfunction3012267350-2025-00001
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3012267350.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Sep 27, 2024
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Sep 27, 2024
Postmarket Assurance: Devices · Citations posted
Inspection citations
6 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.22Sep 27, 2024
Quality Audit/Reaudit - documentation
- 21 CFR 820.40Sep 27, 2024
Procedures not adequately established or maintained
- 21 CFR 820.100(a)Sep 27, 2024
Lack of or inadequate procedures
- 21 CFR 820.100(b)Sep 27, 2024
Documentation
- 21 CFR 820.198(a)Sep 27, 2024
Complaints
- 21 CFR 820.198(a)Sep 27, 2024
Lack of or inadequate complaint procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.