Company
United StatesAcuderm, Inc., Ft Lauderdale, FL – FDA Inspections
Inspection records and compliance data for Acuderm, Inc. in Ft Lauderdale, Florida. 3 FDA inspections on record, 1 Form 483, last inspected July 13, 2017.
Company Profile
This profile covers Acuderm, Inc. based in Ft Lauderdale, Florida, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 3
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
First inspected February 19, 2010. Last inspected July 13, 2017.
Most cited issue areas
- Calibration, Inspection, etc. Procedures Lack of or Inadequ2 inspections
- Documentation2 inspections
- Purchasing controls, Lack of or inadequate procedures2 inspections
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| July 13, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1017933 |
| May 9, 2014 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 878759 |
| February 19, 2010 | VAI | Medical Devices & Rad Health · Compliance: Devices | 646620 |
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
Acuderm, Inc.
FEI Number
1035236
Address
6555 Powerline Rd, Ft Lauderdale, Florida 33309, United States
Country
United States
ID: 9dd97a4d-a9f0-4ae2-8c49-d9b4765fe034