FDA Inspection 1249138 — Karl Storz Endoscopy

Karl Storz Endoscopy — FEI 3007475226

The FDA completed an inspection of Karl Storz Endoscopy on September 12, 2024 in El Segundo, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 12, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
El Segundo, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
73221 CFR 803.50(a)(2)Individual Report of Malfunction