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
Compliance: Devices
Location
Cedar Rapids, IA (United States)