Labverity
Facility profile

PEKANA Naturheilmittel GmbH

Drug product manufacturing · Kisslegg · Germany

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

Manufacture
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Oct 10, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history6 inspection records

FDA inspection history

6 records, Oct 2008 – Oct 2024 · 0 NAI · 6 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 10, 2024VAIDrug Quality Assurance2025
Jul 22, 2021VAIDrug Quality Assurance2021
Jun 1, 2018VAIDrug Quality AssuranceYes2018
May 6, 2016VAIDrug Quality Assurance2016
Mar 8, 2013VAIDrug Quality AssuranceYes2013
Oct 2, 2008VAIDrug Quality AssuranceYes2009

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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