# LEK d.d., Lendava/Lendva, Slovenia – FDA Inspections

Source: https://www.keypedia.com/companies/lek-dd/49b1b882-f72b-4d83-b4b6-d6e117f97274

> Inspection records and compliance data for LEK d.d. in Lendava/Lendva. 6 FDA inspections on record, last inspected April 10, 2026.

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## Details

- Name: LEK d.d.
- FEI Number: 3002807463
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Trimlini 2d
- City: Lendava/Lendva
- Country Name: Slovenia
- Address: Trimlini 2d, Lendava/Lendva, Slovenia
- Country: Slovenia

## Related Documents

- FDA Inspection 1319066 - LEK d.d. - 2026-04-10 — source: FDA, date: April 10, 2026
- FDA Inspection 1271780 - LEK d.d. - 2022-11-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 24, 2022
- FDA Inspection 1123872 - LEK d.d. - 2019-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2019
- FDA Inspection 945705 - LEK d.d. - 2015-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2015
- FDA Inspection 807392 - LEK d.d. - 2012-10-12 — classification: No Action Indicated (NAI), source: FDA, date: October 12, 2012
- FDA Inspection 548049 - LEK d.d. - 2008-11-11 — classification: No Action Indicated (NAI), source: FDA, date: November 11, 2008

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