# Archimica S.p.A, Lodi, Italy – FDA Inspections

Source: https://www.keypedia.com/companies/archimica-spa/4dd6ea31-d4ed-4966-a8f5-c27da742f2ca

> Inspection records and compliance data for Archimica S.p.A in Lodi. 6 FDA inspections on record, 1 Form 483, last inspected June 15, 2023.

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## Details

- Name: Archimica S.p.A
- FEI Number: 3002874947
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Viale Milano 86
- City: Lodi
- Country Name: Italy
- Address: Viale Milano 86, Lodi, Italy
- Country: Italy

## Related Documents

- FDA Inspection 1220541 - Archimica S.p.A - 2023-06-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2023
- FDA Inspection 1123733 - Archimica S.p.A - 2018-09-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2018
- FDA Inspection 1094988 - Archimica S.p.A - 2017-07-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2017
- [FDA Inspection 1013470 - Archimica S.p.A - 2017-04-28](https://www.keypedia.com/records/fda_inspections/archimica-spa/b69db2c0-61bd-40d2-ac41-184c857cabde) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2017
- FDA Inspection 900514 - Archimica S.p.A - 2014-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2014
- [FDA Inspection 744980 - Archimica S.p.A - 2011-09-08](https://www.keypedia.com/records/fda_inspections/archimica-spa/2e1bf043-158e-46e7-a8c9-787e4ccdbaea) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2011

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