Company
United StatesKindara, Boulder, CO – FDA Inspections
Inspection records and compliance data for Kindara in Boulder, CO. 1 FDA inspection on record, 1 Form 483, last inspected February 08, 2017.
Company Profile
This profile covers Kindara based in Boulder, CO, United States.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected February 8, 2017.
Most cited issue areas
- Design transfer - Lack of or inadequate procedures1 inspection
- Design validation - documentation1 inspection
- Design validation - software validation not performed1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| February 8, 2017 | Not classified | Medical Devices & Rad Health · Compliance: Devices | 1001292 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Kindara
FEI Number
3012151765
Address
2560 28th St Ste 102, Boulder, CO 80301-1244, United States
Country
United States
ID: b80dae50-851a-4a2c-ae82-5a63a6f51278