Company
United StatesReNovo, Inc., Bend, OR – FDA Inspections
Inspection records and compliance data for ReNovo, Inc. in Bend, Oregon. 2 FDA inspections on record (1 OAI), 2 Form 483s, 1 warning letter, last inspected May 18, 2023.
Company Profile
This profile covers ReNovo, Inc. based in Bend, Oregon, United States.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 1
- VAI
- 0
- NAI
- 1
- Form 483s
- 2
- Warning letters
- 1
First inspected June 21, 2018. Last inspected May 18, 2023.
Most cited issue areas
- Environmental control Lack of or inadequate procedures1 inspection
- Nonconforming product, Lack of or inadequate procedures1 inspection
- Periodic equipment inspection lack of or inadequate procedu1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 18, 2023 | OAI | Medical Devices & Rad Health · Compliance: Devices | 1205740 |
| June 21, 2018 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1057926 |
FDA documents
Form 483s (2)
Warning Letters (1)
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
ReNovo, Inc.
FEI Number
3014023545
Address
340 Sw Columbia St, Bend, Oregon 97702, United States
Country
United States
ID: 05b78813-dfe4-488e-b1f9-624731d7205d