FDA Inspection 883813 — CareHealth America DBA Express Diagnostics International

CareHealth America DBA Express Diagnostics International — FEI 3014946040

The FDA completed an inspection of CareHealth America DBA Express Diagnostics International on June 24, 2014 in Blue Earth, MN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 24, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Blue Earth, MN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312321 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation