MEDA Manufacturing GmbH FDA Record

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

MEDA Manufacturing GmbH has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "MEDA Manufacturing GmbH" is on file.

What these totals cover: FDA records filed under the name "MEDA Manufacturing GmbH" and its spelling variant "Meda Manufacturing".

Latest inspection
Sep 7, 2017 · VAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

5 inspections from Jan 30, 2009 to Sep 7, 2017.

DateSiteProductClassificationFEI
Sep 7, 2017Cologne, GermanyDrugsVoluntary Action Indicated (VAI)3002808393
Sep 9, 2016Cologne, GermanyVeterinaryNo Action Indicated (NAI)3002808393
Jul 18, 2014Merignac, FranceDrugsNo Action Indicated (NAI)3009324649
Nov 22, 2013Cologne, GermanyDrugsNo Action Indicated (NAI)3002808393
Jan 30, 2009Cologne, GermanyVeterinaryNo Action Indicated (NAI)3002808393
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.

FacilityLocationInspectionsLatest
FEI 3002808393Cologne, Germany4Sep 7, 2017
FEI 3009324649Merignac, France1Jul 18, 2014

MEDA Manufacturing GmbH and the FDA: common questions

Has MEDA Manufacturing GmbH received an FDA warning letter?

No FDA warning letter addressed to the name "MEDA Manufacturing GmbH" 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 MEDA Manufacturing GmbH received an FDA Form 483?

FDA has not published a Form 483 for "MEDA Manufacturing GmbH" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect MEDA Manufacturing GmbH?

The most recent FDA inspection on file ended Sep 7, 2017 at Cologne, Germany and was classified VAI. FDA has 5 inspections of MEDA Manufacturing GmbH on file.

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