Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International FDA Record
- Latest inspection VAI · Dec 7, 2012
- No warning letters matched by name
Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International" is on file.
- Latest inspection
- Dec 7, 2012 · VAI
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 0 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 3 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Reviewing Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or check Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Recent FDA inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Dec 7, 2012 | Bern, Switzerland | Biologics | Voluntary Action Indicated (VAI) | 3012991344 |
| Feb 25, 2011 | Bern, Switzerland | Biologics | Voluntary Action Indicated (VAI) | 3012991344 |
| Jan 23, 2009 | Bern, Switzerland | Biologics | Voluntary Action Indicated (VAI) | 3012991344 |
- 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.
FDA-inspected facilities
| Facility | Location | Inspections | Latest |
|---|---|---|---|
| FEI 3012991344 | Bern, Switzerland | 3 | Dec 7, 2012 |
Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International and the FDA: common questions
Has Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International received an FDA warning letter?
No FDA warning letter addressed to the name "Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International" 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 Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International received an FDA Form 483?
FDA has not published a Form 483 for "Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International" in its reading room. FDA publishes some Form 483s, not all of them.
When did the FDA last inspect Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International?
The most recent FDA inspection on file ended Dec 7, 2012 at Bern, Switzerland and was classified VAI. FDA has 3 inspections of Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International on file.
Need more than this page shows? Ask about Janssen Vaccines, Zweigniederlassung Der Cilag GmbH International in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.