FEI 1000221463
Medical Instrument Development Laboratories, Inc.
557 McCormick St, SAN LEANDRO, CA, US
MDR events19All time
Recalls0All time
Registered products6
Establishment typeManufactureManufacture Medical Device
Registered product codes
6 product codes
Recent MDR events
19 on file
- MID LABSJan 27, 2016Malfunction2935428-2016-00004
- MID LABSJan 27, 2016Malfunction2935428-2016-00003
- MID LABSJan 27, 2016Malfunction2935428-2016-00002
- MID LABSJan 27, 2016Malfunction2935428-2016-00001
- MID LABSAug 28, 2015Malfunction2935428-2015-00001
- MID LABSAug 28, 2015Malfunction2935428-2015-00002
- MIDLABS VITROUS CUTTERAug 28, 2015Malfunction2935428-2015-00003
- MIDLABSAug 28, 2015Malfunction2935428-2015-00004
- MID LABSMay 11, 2012Malfunction2935428-2012-00001
- MID LABSMay 11, 2012Malfunction2935428-2012-00002
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 1000221463.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Aug 13, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Aug 13, 2025
Postmarket Assurance: Devices · Citations posted
Inspection citations
4 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.30(c)Aug 13, 2025
Design input - Lack of or inadequate procedures
- 21 CFR 820.90(b)(2)Aug 13, 2025
Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.100(a)Aug 13, 2025
Lack of or inadequate procedures
- 21 CFR 820.198(a)Aug 13, 2025
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.