Company
Korea (the Republic of)Interojo Inc., Pyeongtaek City, Korea (the Republic of) – FDA Inspections
Inspection records and compliance data for Interojo Inc. in Pyeongtaek City. 3 FDA inspections on record, 2 Form 483s, 1 warning letter, last inspected August 29, 2019.
Company Profile
This profile covers Interojo Inc. based in Pyeongtaek City, Korea (the Republic of).
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 2
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 2
- Warning letters
- 1
First inspected July 18, 2013. Last inspected August 29, 2019.
Most cited issue areas
- DHR - not or inadequately maintained1 inspection
- DHR - UDI not included1 inspection
- Documentation1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| August 29, 2019 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1101815 |
| September 7, 2018 | Not classified | Medical Devices & Rad Health | 1124008 |
| July 18, 2013 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 848893 |
FDA documents
Warning Letters (1)
People (1)
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Interojo Inc.
FEI Number
3004146030
Address
28 25 Sandan-Ro 15 Beon-Gil, Pyeongtaek City, Korea (the Republic of)
Country
Korea (the Republic of)
ID: afd7a693-fcdd-4cc6-81cc-423cfcc2e392