Company
Dominican Republic (the)Arjo Dominican Republic, Itabo, Haina, Dominican Republic (the) – FDA Inspections
Inspection records and compliance data for Arjo Dominican Republic in Itabo, Haina. 1 FDA inspection on record, 1 Form 483, last inspected May 28, 2026.
Company Profile
This profile covers Arjo Dominican Republic based in Itabo, Haina, Dominican Republic (the).
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected May 28, 2026.
Most cited issue areas
- Design and development validation not complete prior to release of product1 inspection
- Process for production and service provision not validated1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 28, 2026 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1319304 |
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
Arjo Dominican Republic
FEI Number
3012292104
Address
Building 9, 7 & 21 Piisa Industrial Park, Km. 18 1/2 Antigua Carretera Sanchez, Itabo, Haina, Dominican Republic (the)
Country
Dominican Republic (the)
ID: 4b82d031-7fd5-4d28-98b3-f9584ecef540