# Redox S.r.l. – FDA Inspection, Apr 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/redox-srl/fd5c2b86-cb6a-4a56-83c1-ec3eb7733344
Source feed: FDA_Inspections

> FDA inspection 1090329 of Redox S.r.l., April 12, 2019. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1090329
- Company Name: Redox S.r.l.
- Inspection Date: 2019-04-12
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: Office of Inspections and Investigations
- Citation Count: 0

## Related Documents

- FDA Inspection 1269520 - 2023-03-08
- FDA Inspection 1119645 - 2019-05-24
- [FDA Inspection 917270 - 2015-02-20](https://www.keypedia.com/records/fda_inspections/redox-srl/7adebe31-c39f-4128-9ff1-b09eefa5b77c)
- FDA Inspection 747478 - 2011-09-28

## Related Officers

- [Company Rep](https://www.keypedia.com/people/amir-alavi/d7179128-eb3f-489e-97cf-e2c5e5539a00)
- Issuing Officer

Company: https://www.keypedia.com/companies/redox-srl/7c0f1e45-bf6f-4fe9-a532-8af6b8b8515d

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