935564

Med-Mizer, Inc. — FEI 3004976058

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 6, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Batesville, IN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures
1471521 CFR 820.30(d)Design output - Lack of or inadequate procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
260421 CFR 820.30(e)Design review - Lack of or inadequate procedures
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
310421 CFR 820.30(j)Design history file
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
330921 CFR 820.120(b)Examination for accuracy
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation
63121 CFR 803.17(a)(1)Lack of System for Event Evaluations