FDA Inspection 822147 — Biokit, S.A.

Biokit, S.A. — FEI 3002806557

The FDA completed an inspection of Biokit, S.A. on Feb 21, 2013 in Llica D'Amunt. 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 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Llica D'Amunt (Spain)

Citations

IDCFRDescription
54621 CFR 820.75(a)Lack of or inadequate process validation