# Nobilus Ent Oddzial Kutno - Inspection Records

Source: https://www.globalkeysolutions.net/companies/nobilus-ent-oddzial-kutno/f3113759-ba51-4720-b2b9-df3f6473888c

> Inspection records and compliance data for Nobilus Ent Oddzial Kutno in Kutno, None. Access full analysis and detailed observations.

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## Details

- Name: Nobilus Ent Oddzial Kutno
- FEI Number: 3008517755
- City: Kutno
- State: None
- Country Name: Poland
- Address Line 1: Ul. Metalowa 6a
- Zip Code: None
- Business Operations: API MANUFACTURE

## Related Documents

- [FDA Inspection 1280241 - Nobilus Ent Oddzial Kutno - 2024-05-09](https://www.globalkeysolutions.net/records/fda_inspections/nobilus-ent-oddzial-kutno/054ba117-0014-468e-9281-8cfb70fe9890) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2024
- [FDA Inspection 1172869 - Nobilus Ent Oddzial Kutno - 2019-07-11](https://www.globalkeysolutions.net/records/fda_inspections/nobilus-ent-oddzial-kutno/0869ccbd-fe6b-4ff7-80a9-b958f038b8f1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2019
- [FDA Inspection 1032067 - Nobilus Ent Oddzial Kutno - 2017-09-15](https://www.globalkeysolutions.net/records/fda_inspections/nobilus-ent-oddzial-kutno/fef955db-e401-4e60-a18f-f450024556f1) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2017
- [FDA Inspection 910059 - Nobilus Ent Oddzial Kutno - 2014-12-18](https://www.globalkeysolutions.net/records/fda_inspections/nobilus-ent-oddzial-kutno/aa3e136a-5ca4-4f27-bdc3-24f197dab6bc) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- [WARNING_LETTER - Nobilus Ent Oddzial Kutno - 2011-09-15](https://www.globalkeysolutions.net/records/warning_letter/nobilus-ent-oddzial-kutno/a2498568-9426-4080-adb3-22666ba3d11d) — source: FDA, date: September 15, 2011
- [FDA Inspection 749420 - Nobilus Ent Oddzial Kutno - 2011-09-15](https://www.globalkeysolutions.net/records/fda_inspections/nobilus-ent-oddzial-kutno/3d392de6-9344-4bf4-89d1-f9e86adcb078) — classification: Official Action Indicated (OAI), source: FDA, date: September 15, 2011

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