FDA Inspection 1059960 — Nypro, Inc.

Nypro, Inc. — FEI 3011024991

The FDA completed an inspection of Nypro, Inc. on Jun 27, 2018 in Maple Grove, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)