FDA Inspection 941493 — Perryman Company

Perryman Company — FEI 3009882462

The FDA completed an inspection of Perryman Company on September 10, 2015 in Houston, PA. 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
September 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, PA (United States)