# Latina Pharma S.p.A. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/latina-pharma-spa/9cb7e758-39a0-4b4c-bfad-93d1468f5d38

> Inspection records and compliance data for Latina Pharma S.p.A. in Latina, None. Access full analysis and detailed observations.

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## Details

- Name: Latina Pharma S.p.A.
- FEI Number: 3001229385
- City: Latina
- State: None
- Country Name: Italy
- Address Line 1: Via del Murillo Km 2
- Address Line 2: 800, Sermoneta
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - Latina Pharma S.p.A. - Unknown Date](https://www.globalkeysolutions.net/records/483/latina-pharma-spa/5b49a901-90de-4304-b852-d0b8f1913e86) — source: FDA, date: Invalid Date
- [FDA Inspection 1240979 - Latina Pharma S.p.A. - 2024-01-19](https://www.globalkeysolutions.net/records/fda_inspections/latina-pharma-spa/0c906181-5ab3-4c1e-962a-170d3c3a8140) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 19, 2024
- [FDA Inspection 1109198 - Latina Pharma S.p.A. - 2019-09-27](https://www.globalkeysolutions.net/records/fda_inspections/latina-pharma-spa/b7db89e5-40ed-4dca-b8ae-451db5f4e4f7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2019
- [FDA Inspection 1018753 - Latina Pharma S.p.A. - 2017-04-21](https://www.globalkeysolutions.net/records/fda_inspections/latina-pharma-spa/bd105b3b-7a93-45a0-8b44-c0a1d325293b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2017
- [FDA Inspection 928171 - Latina Pharma S.p.A. - 2015-05-29](https://www.globalkeysolutions.net/records/fda_inspections/latina-pharma-spa/e1f220e4-6ffd-4e0b-9ab0-185bf35a73ee) — classification: Official Action Indicated (OAI), source: FDA, date: May 29, 2015
- [FDA Inspection 844700 - Latina Pharma S.p.A. - 2013-07-24](https://www.globalkeysolutions.net/records/fda_inspections/latina-pharma-spa/ee7b1d4a-f2e5-40d2-9fc2-a8c51047599e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2013

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