FDA inspection

Zimmer Manufacturing B.V.: FDA inspection ending Oct 1, 2020

FDA inspection 1133679 · No Action Indicated (NAI) · Mercedita, PR

Key facts

Inspection ID 1133679
Firm Zimmer Manufacturing B.V.
FEI number 1000132037
Address Turpeaux Industrial Park, Road 1 Km. 123.4
City Mercedita
State PR
ZIP 00715
Country United States
Fiscal year 2021
Inspection end date Oct 1, 2020
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections