FDA Inspection 705980 — Aerscher Diagnostics, LLC

Aerscher Diagnostics, LLC — FEI 1000219815

The FDA completed an inspection of Aerscher Diagnostics, LLC on January 19, 2011 in Chestertown, MD. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 19, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Chestertown, MD (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312721 CFR 820.80(e)Documentation
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
341521 CFR 820.22Quality Audit/Reaudit - conducted
53721 CFR 820.70(a)Production processes