FDA Inspection 786506 — Acp Of Delaware Inc.

Acp Of Delaware Inc. — FEI 2000006313

The FDA completed an inspection of Acp Of Delaware Inc. on June 14, 2012 in Cedar Rapids, IA. 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
June 14, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Cedar Rapids, IA (United States)