# LEK d.d. - Inspection Records

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

> Inspection records and compliance data for LEK d.d. in Prevalje, None. Access full analysis and detailed observations.

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## Details

- Name: LEK d.d.
- FEI Number: 3003706290
- City: Prevalje
- State: None
- Country Name: Slovenia
- Address Line 1: Perzonali 47
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING, PACK, REPACK

## Related Documents

- [FDA Inspection 1277489 - LEK d.d. - 2024-10-02](https://www.keypedia.com/records/fda_inspections/lek-dd/b25597c0-284d-4c86-9c87-8672ac6a412e) — source: FDA, date: October 2, 2024
- [FDA Inspection 1277489 - LEK d.d. - 2024-10-02](https://www.keypedia.com/records/fda_inspections/lek-dd/839e6048-5c7e-481d-8722-944d34d548d7) — classification: No Action Indicated (NAI), source: FDA, date: October 2, 2024
- [FDA Inspection 1123337 - LEK d.d. - 2019-03-14](https://www.keypedia.com/records/fda_inspections/lek-dd/d532f4ac-080b-4b61-9003-b15f9bcb8a38) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 14, 2019
- [FDA Inspection 892528 - LEK d.d. - 2014-07-17](https://www.keypedia.com/records/fda_inspections/lek-dd/ac8aeb03-a4ba-413e-95a0-88ab922bc532) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2014
- [FDA Inspection 785881 - LEK d.d. - 2012-05-17](https://www.keypedia.com/records/fda_inspections/lek-dd/c2e937b0-14d1-40ec-b925-66ae97bd7298) — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2012

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