FDA inspection

Rommelag CDMO GmbH: FDA inspection ending Feb 18, 2020

FDA inspection 1118070 · No Action Indicated (NAI) · Sulzbach-Laufen

Key facts

Inspection ID 1118070
Firm Rommelag CDMO GmbH
FEI number 3002808845
Address Bahnhofstr. 18
City Sulzbach-Laufen
Country Germany
Fiscal year 2020
Inspection end date Feb 18, 2020
Classification No Action Indicated (NAI)
Project area Pre-Approval Eval. of Animal Drugs and Food Additives
Product type Veterinary

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

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

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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