1053624

Lusys Laboratories, Inc. — FEI 3004473533

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
1472021 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
1472221 CFR 820.40Procedures not adequately established or maintained
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate
368321 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
383721 CFR 820.25(b)Training records
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures