FDA Inspection 1297858 — Esco Medical Technologies Ltd.

Esco Medical Technologies Ltd. — FEI 3009747883

The FDA completed an inspection of Esco Medical Technologies Ltd. on January 8, 2026 in Ramuciai. 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
January 8, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Ramuciai (Lithuania)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
63021 CFR 803.17Lack of Written MDR Procedures