Company
United StatesScanlan International, Inc., Saint Paul, MN – FDA Inspections
Inspection records and compliance data for Scanlan International, Inc. in Saint Paul, Minnesota. 4 FDA inspections on record, last inspected August 15, 2019.
Company Profile
This profile covers Scanlan International, Inc. based in Saint Paul, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 0
- NAI
- 4
- Form 483s
- 0
- Warning letters
- 0
First inspected June 22, 2010. Last inspected August 15, 2019.
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| August 15, 2019 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1100869 |
| February 3, 2016 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1007424 |
| October 17, 2012 | NAI | Medical Devices & Rad Health · Compliance: Devices | 803860 |
| June 22, 2010 | NAI | Medical Devices & Rad Health · Compliance: Devices | 667421 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Scanlan International, Inc.
FEI Number
2126670
Address
1 Scanlan Plz, Saint Paul, Minnesota 55107, United States
Country
United States
ID: aa92ea7e-de23-46bc-8fdc-6cacefac2c83