CIPAN - Companhia Industrial Produtora De Antibioticos SA FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • Latest inspection VAI · Feb 9, 2023
  • No warning letters matched by name
Inspections 6 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

CIPAN - Companhia Industrial Produtora De Antibioticos SA has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "CIPAN - Companhia Industrial Produtora De Antibioticos SA" is on file.

What these totals cover: FDA records filed under the name "CIPAN - Companhia Industrial Produtora De Antibioticos SA" and its spelling variant "Cipan - Companhia Industrial Produtora De Antibioticos".

Latest inspection
Feb 9, 2023 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections6Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

CIPAN - Companhia Industrial Produtora De Antibioticos SA's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

CIPAN - Companhia Industrial Produtora De Antibioticos SA: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202310000
202200000
202100000
202010000
201900000
201810000
201700000

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.

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Recent FDA inspections

6 inspections from Oct 1, 2009 to Feb 9, 2023.

DateSiteProductClassificationFEI
Feb 9, 2023Castanheira Do Ribatejo, PortugalDrugsVoluntary Action Indicated (VAI)3002806694
Feb 21, 2020Castanheira Do Ribatejo, PortugalDrugsVoluntary Action Indicated (VAI)3002806694
Feb 23, 2018Castanheira Do Ribatejo, PortugalDrugsNo Action Indicated (NAI)3002806694
Nov 6, 2015Castanheira Do Ribatejo, PortugalDrugsVoluntary Action Indicated (VAI)3002806694
Dec 8, 2011Castanheira Do Ribatejo, PortugalDrugsVoluntary Action Indicated (VAI)3002806694
Oct 1, 2009Castanheira Do Ribatejo, PortugalDrugsNo Action Indicated (NAI)3002806694
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

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3002806694Castanheira Do Ribatejo, Portugal6Feb 9, 2023

CIPAN - Companhia Industrial Produtora De Antibioticos SA and the FDA: common questions

Has CIPAN - Companhia Industrial Produtora De Antibioticos SA received an FDA warning letter?

No FDA warning letter addressed to the name "CIPAN - Companhia Industrial Produtora De Antibioticos SA" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has CIPAN - Companhia Industrial Produtora De Antibioticos SA received an FDA Form 483?

FDA has not published a Form 483 for "CIPAN - Companhia Industrial Produtora De Antibioticos SA" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect CIPAN - Companhia Industrial Produtora De Antibioticos SA?

The most recent FDA inspection on file ended Feb 9, 2023 at Castanheira Do Ribatejo, Portugal and was classified VAI. FDA has 6 inspections of CIPAN - Companhia Industrial Produtora De Antibioticos SA on file.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.