# Catalent Argentina S.A.I.C. - Inspection Records

Source: https://www.keypedia.com/companies/catalent-argentina-saic/c4e097df-85fe-4836-9778-b395fe1e78de

> Inspection records and compliance data for Catalent Argentina S.A.I.C. in Buenos Aires, None. Access full analysis and detailed observations.

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## Details

- Name: Catalent Argentina S.A.I.C.
- FEI Number: 3004258511
- City: Buenos Aires
- State: None
- Country Name: Argentina
- Address Line 1: 691 Villa Loma Hermosa, Av. Bernabe Marquez
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE

## Related Documents

- [483 - Catalent Argentina S.A.I.C. - 2023-08-04](https://www.keypedia.com/records/483/catalent-argentina-saic/cbabcbc7-9031-467b-b457-3a7b2e4658bc) — source: FDA, date: August 4, 2023
- [FDA Inspection 1211696 - Catalent Argentina S.A.I.C. - 2023-08-04](https://www.keypedia.com/records/fda_inspections/catalent-argentina-saic/e10e4c3b-0e97-4036-b601-c71316d2ee91) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2023
- [FDA Inspection 1038458 - Catalent Argentina S.A.I.C. - 2017-12-22](https://www.keypedia.com/records/fda_inspections/catalent-argentina-saic/379e6ec4-d624-4069-9ad6-8c21d6f07d68) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 22, 2017
- [FDA Inspection 881348 - Catalent Argentina S.A.I.C. - 2014-05-16](https://www.keypedia.com/records/fda_inspections/catalent-argentina-saic/bbc6d871-6804-4a14-8d3f-9768cae31e68) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2014
- [FDA Inspection 803767 - Catalent Argentina S.A.I.C. - 2012-09-14](https://www.keypedia.com/records/fda_inspections/catalent-argentina-saic/c2d2ad76-6fb6-4ec3-bbc4-f03052901f5d) — classification: No Action Indicated (NAI), source: FDA, date: September 14, 2012
- [FDA Inspection 604132 - Catalent Argentina S.A.I.C. - 2009-07-02](https://www.keypedia.com/records/fda_inspections/catalent-argentina-saic/8d3c133e-b0c3-4176-b63c-a41cd415cc7c) — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2009

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