ACTEON MANUFACTURING — FDA Facility Profile

FEI 3003677417

ACTEON MANUFACTURING is an FDA-registered facility (FEI 3003677417) located in Merignac Gironde, FR. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing ACTEON MANUFACTURING 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.

Check this supplier

Or check ACTEON MANUFACTURING yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Facility Details

Location
Merignac Gironde (FR)
Source
device

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