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Anidro Do Brasil Extracoes S.A.

FDA Regulatory Profile

Anidro Do Brasil Extracoes S.A. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Anidro Do Brasil Extracoes S.A." and its spelling variant "Anidro Do Brasil Extracoes".

Latest inspection: Nov 15, 2024 · VAI

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Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	6	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Anidro Do Brasil Extracoes S.A.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	0	0	0	0
2024	1	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

6 inspections from May 13, 2010 to Nov 15, 2024.

Date	Site	Product	Classification	FEI
Nov 15, 2024	Parnaiba, Brazil	Drugs	Voluntary Action Indicated (VAI)	3002807563
Oct 25, 2019	Parnaiba, Brazil	Drugs	Voluntary Action Indicated (VAI)	3002807563
Dec 14, 2016	Parnaiba, Brazil	Drugs	Voluntary Action Indicated (VAI)	3002807563
Mar 17, 2015	Botucatu, Brazil	Food/Cosmetics	No Action Indicated (NAI)	3011411233
Sep 20, 2012	Parnaiba, Brazil	Drugs	Voluntary Action Indicated (VAI)	3002807563
May 13, 2010	Parnaiba, Brazil	Drugs	Voluntary Action Indicated (VAI)	3002807563

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

2 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3002807563	Parnaiba, Brazil	5	Nov 15, 2024
FEI 3011411233	Botucatu, Brazil	1	Mar 17, 2015

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