FDA Inspection 834402 — Halyard North Carolina, LLC

Halyard North Carolina, LLC — FEI 1000110722

The FDA completed an inspection of Halyard North Carolina, LLC on June 3, 2013 in Linwood, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 3, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Linwood, NC (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures