# Intercos Europe SpA – FDA Inspection, Nov 29, 2024

Source: https://www.keypedia.com/records/fda_inspections/intercos-europe-spa/79ad9350-4d62-463c-9eea-d50e2b29c32d
Source feed: FDA_Inspections

> FDA inspection 1256045 of Intercos Europe SpA, November 29, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1256045
- Company Name: Intercos Europe SpA
- Inspection Date: 2024-11-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 1110083 - 2019-09-11
- [FDA Inspection 978093 - 2016-06-24](https://www.keypedia.com/records/fda_inspections/intercos-europe-spa/19a275e6-3f46-4c9d-856f-047773743fc4)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/lisa-r-hilliard/611735cf-5c20-424c-801a-03888d8d1b0a)

Company: https://www.keypedia.com/companies/intercos-europe-spa/8fa65017-2fc9-4fd3-8665-63c2c31493f1

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8