FDA Inspection 1292176 — Olympus Winter & IBE Gmbh

Olympus Winter & IBE Gmbh — FEI 3002807798

The FDA completed an inspection of Olympus Winter & IBE Gmbh on Nov 21, 2025 in Hamburg. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Nov 21, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hamburg (Germany)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
319221 CFR 820.30(g)Design validation - user needs and intended uses
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
73221 CFR 803.50(a)(2)Individual Report of Malfunction