# LEK d.d., Prevalje, Slovenia – FDA Inspections

Source: https://www.keypedia.com/companies/lek-dd/c0d31ce7-5f89-4795-8f41-03edc49e6e35

> Inspection records and compliance data for LEK d.d. in Prevalje. 5 FDA inspections on record, last inspected October 02, 2024.

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## Details

- Name: LEK d.d.
- FEI Number: 3003706290
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK, REPACK
- Address Line 1: Perzonali 47
- City: Prevalje
- Country Name: Slovenia
- Address: Perzonali 47, Prevalje, Slovenia
- Country: Slovenia

## Related Documents

- FDA Inspection 1277489 - LEK d.d. - 2024-10-02 — source: FDA, date: October 2, 2024
- FDA Inspection 1277489 - LEK d.d. - 2024-10-02 — classification: No Action Indicated (NAI), source: FDA, date: October 2, 2024
- FDA Inspection 1123337 - LEK d.d. - 2019-03-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2019
- FDA Inspection 1035459 - LEK d.d. - 2017-09-29 — source: FDA, date: September 29, 2017
- FDA Inspection 892528 - LEK d.d. - 2014-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2014
- FDA Inspection 785881 - LEK d.d. - 2012-05-17 — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2012

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