Company
United StatesRespicardia, Inc., Minnetonka, MN – FDA Inspections
Inspection records and compliance data for Respicardia, Inc. in Minnetonka, Minnesota. 3 FDA inspections on record, 1 Form 483, last inspected March 22, 2024.
Company Profile
This profile covers Respicardia, Inc. based in Minnetonka, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 1
- NAI
- 2
- Form 483s
- 1
- Warning letters
- 0
First inspected June 4, 2015. Last inspected March 22, 2024.
Most cited issue areas
- Sponsors' general responsibilities1 inspection
- Sponsors" general responsibilities1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| March 22, 2024 | NAI | Medical Devices & Rad Health · Compliance: Devices | 1235640 |
| February 13, 2017 | VAI | Medical Devices & Rad Health · Bioresearch Monitoring | 1006033 |
| June 4, 2015 | NAI | Medical Devices & Rad Health · Compliance: Devices | 929406 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Respicardia, Inc.
FEI Number
3009144177
Address
12400 Whitewater Dr Ste 150, Minnetonka, Minnesota 55343, United States
Country
United States
ID: 495d9041-03c9-4c3b-a405-63b7ddef0219