FDA Inspection 708621 — J Hugh Knight Instrument Co Inc

J Hugh Knight Instrument Co Inc — FEI 3002691692

The FDA completed an inspection of J Hugh Knight Instrument Co Inc on Feb 3, 2011 in Slidell, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 3, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Slidell, LA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures