MedOffice Saglik Endustri Anonim Sirketi FDA Record

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

  • Latest inspection OAI · May 10, 2024
  • Last warning letter 2024
Inspections 1 1 OAI
Recalls 0 0 Class I
Warning letters 1 Latest Oct 23, 2024
510(k) clearances 0 None on file

MedOffice Saglik Endustri Anonim Sirketi has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to MedOffice Saglik Endustri Anonim Sirketi, the most recent on Oct 23, 2024.

What these totals cover: FDA records filed under the name "MedOffice Saglik Endustri Anonim Sirketi".

Latest inspection
May 10, 2024 · OAI

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
Inspections1Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

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MedOffice Saglik Endustri Anonim Sirketi FDA Warning Letters

1 warning letter on Oct 23, 2024.

IssuedSubjectIssuing officeClose-out letter
Oct 23, 2024 · Letter on fda.gov CGMP/Finished Pharmaceuticals/AdulteratedCenter for Drug Evaluation and Research (CDER)

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

1 inspection on May 10, 2024.

DateSiteProductClassificationFEI
May 10, 2024Torbali, TurkeyDrugsOfficial Action Indicated (OAI)3019167311
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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under MedOffice Saglik Endustri Anonim Sirketi: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Oct 23, 2024.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3019167311Torbali, Turkey1May 10, 2024

MedOffice Saglik Endustri Anonim Sirketi and the FDA: common questions

Has MedOffice Saglik Endustri Anonim Sirketi received an FDA warning letter?

Yes. FDA has issued 1 warning letter to MedOffice Saglik Endustri Anonim Sirketi. The most recent is dated Oct 23, 2024, with the subject "CGMP/Finished Pharmaceuticals/Adulterated".

Has MedOffice Saglik Endustri Anonim Sirketi received an FDA Form 483?

FDA has not published a Form 483 for "MedOffice Saglik Endustri Anonim Sirketi" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect MedOffice Saglik Endustri Anonim Sirketi?

The most recent FDA inspection on file ended May 10, 2024 at Torbali, Turkey and was classified OAI. FDA has 1 inspection of MedOffice Saglik Endustri Anonim Sirketi on file, 1 of them classified OAI (official action indicated).

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