FDA Inspection 1133679 — Zimmer Manufacturing B.V.

Zimmer Manufacturing B.V. — FEI 1000132037

The FDA completed an inspection of Zimmer Manufacturing B.V. on October 1, 2020 in Mercedita, PR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 1, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Mercedita, PR (United States)