FDA Inspection 898410 — Combo AG

Combo AG — FEI 3009625473

The FDA completed an inspection of Combo AG on September 11, 2014 in Langendorf. 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
September 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Langendorf (Switzerland)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
44721 CFR 820.40Lack of procedures, or not maintained