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Facility profile

Ophtapharm AG

Testing & analysis · Drug product manufacturing · Hettlingen · Switzerland

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.

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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)

Feb 28, 2020 · 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 history7 inspection records

FDA inspection history

7 records, Nov 2011 – Feb 2020 · 0 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
Feb 28, 2020VAIDrug Quality AssuranceYes2020
Feb 28, 2020VAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2020
Dec 12, 2017VAIDrug Quality AssuranceYes2018
May 25, 2016VAIMonitoring of Marketed Animal Drugs, Feed, and DevicesYes2016
May 25, 2016VAIDrug Quality AssuranceYes2016
Mar 28, 2014VAIDrug Quality AssuranceYes2014
Nov 9, 2011VAIDrug Quality Assurance2012

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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