Establishment registration

Rommelag CDMO GmbH

FDA establishment registration 9681630 · Sulzbach-Laufen Baden-Wurttemberg, DE

Key facts

Registration number 9681630
Establishment name Rommelag CDMO GmbH
Owner/operator Rommelag CDMO GmbH
Owner/operator number 10028922
FEI number 3002808845
Address Banhofstrasse
City Sulzbach-Laufen Baden-Wurttemberg
Country DE
Establishment types Contract sterilizer
Registration valid through 2026
Product codes listed CAC, FRO, HQD, HQL, KCJ, KDQ, LPN, MVU, NAE, OCC, PLL
Device classes 1, 2, 3, U

At a glance

  • 10–99 Device listings
  • None UDI devices (GUDID)
  • Current Registration current
  • 10–99 FDA inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device establishment registrations

Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device establishment registrations