# FDA Inspection 1291884 - LK Precision AB - November 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/lk-precision-ab/15f2407d-737e-40b9-8d32-995a30388ea0
Source feed: FDA_Inspections

> FDA Inspection 1291884 for LK Precision AB on November 19, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1291884
- Company Name: LK Precision AB
- Inspection Date: 2025-11-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

Company: https://www.keypedia.com/companies/lk-precision-ab/c7f7b8ba-f314-4281-9112-93af002316f1

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8