# FIS - Fabbrica Italiana Sintetici SpA - Inspection Records

Source: https://www.globalkeysolutions.net/companies/fis-fabbrica-italiana-sintetici-spa/37711450-264f-44e9-880f-ccd3809b3dde

> Inspection records and compliance data for FIS - Fabbrica Italiana Sintetici SpA in Lonigo, None. Access full analysis and detailed observations.

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## Details

- Name: FIS - Fabbrica Italiana Sintetici SpA
- FEI Number: 3002808541
- City: Lonigo
- State: None
- Country Name: Italy
- Address Line 1: Almisano Di Lonigo, Via Dovaro 2
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1276304 - FIS - Fabbrica Italiana Sintetici SpA - 2022-10-28](https://www.globalkeysolutions.net/records/fda_inspections/fis-fabbrica-italiana-sintetici-spa/a52ab8bc-c96b-4e51-9dc0-8e54db964a2b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 28, 2022
- [FDA Inspection 1110921 - FIS - Fabbrica Italiana Sintetici SpA - 2019-07-05](https://www.globalkeysolutions.net/records/fda_inspections/fis-fabbrica-italiana-sintetici-spa/12b4b8b3-4d02-4f0f-8201-4c8ac418fc84) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 5, 2019
- [FDA Inspection 961470 - FIS - Fabbrica Italiana Sintetici SpA - 2016-02-25](https://www.globalkeysolutions.net/records/fda_inspections/fis-fabbrica-italiana-sintetici-spa/dc183916-4c26-4ab2-a70c-f9c4ac6ba28a) — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2016
- [FDA Inspection 819321 - FIS - Fabbrica Italiana Sintetici SpA - 2013-02-07](https://www.globalkeysolutions.net/records/fda_inspections/fis-fabbrica-italiana-sintetici-spa/8abb7677-5669-4315-a4fd-ba3d774e5d83) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2013
- [FDA Inspection 650141 - FIS - Fabbrica Italiana Sintetici SpA - 2010-01-22](https://www.globalkeysolutions.net/records/fda_inspections/fis-fabbrica-italiana-sintetici-spa/b4b328e2-f2d9-4569-a043-cbbb0ec0db11) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2010

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