FDA Inspection 1011584 — Linde - Puerto Rico

Linde - Puerto Rico — FEI 1000208816

The FDA completed an inspection of Linde - Puerto Rico on May 4, 2017 in Gurabo, 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
May 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Gurabo, PR (United States)