FDA Inspection 1089793 — Keeler Instruments Inc

Keeler Instruments Inc — FEI 2519784

The FDA completed an inspection of Keeler Instruments Inc on March 18, 2019 in Malvern, 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
March 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Malvern, PA (United States)