Company
United StatesActeon, Inc., Mount Laurel, NJ – FDA Inspections
Inspection records and compliance data for Acteon, Inc. in Mount Laurel, New Jersey. 4 FDA inspections on record, 1 Form 483, last inspected February 23, 2017.
Company Profile
This profile covers Acteon, Inc. based in Mount Laurel, New Jersey, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 1
- NAI
- 3
- Form 483s
- 1
- Warning letters
- 0
First inspected July 9, 2009. Last inspected February 23, 2017.
Most cited issue areas
- Lack of or inadequate procedures - Acceptance activities1 inspection
- Lack of or inadequate receiving acceptance procedures1 inspection
- Process control procedures, Lack of or inadequate procedures1 inspection
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| February 23, 2017 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1002018 |
| December 10, 2014 | VAI | Medical Devices & Rad Health · Compliance: Devices | 905889 |
| December 12, 2011 | NAI | Medical Devices & Rad Health · Compliance: Devices | 756655 |
| July 9, 2009 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 595046 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Acteon, Inc.
FEI Number
2243757
Address
124 Gaither Dr Ste 140, Mount Laurel, New Jersey 08054, United States
Country
United States
ID: 0f7a9961-3060-4c78-97cc-825d4bb4047b