Company
United StatesPENRAD at Sisters Grove Pavilion, Colorado Springs, CO – FDA Inspections
Inspection records and compliance data for PENRAD at Sisters Grove Pavilion in Colorado Springs, CO. 6 FDA inspections on record, last inspected October 28, 2025.
Company Profile
This profile covers PENRAD at Sisters Grove Pavilion based in Colorado Springs, CO, United States.
FDA Inspection History
- FDA inspections
- 6
- OAI
- 0
- VAI
- 0
- NAI
- 0
- Unclassified
- 6
- Form 483s
- 0
- Warning letters
- 0
First inspected September 12, 2017. Last inspected October 28, 2025.
FDA inspections (6)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| October 28, 2025 | Not classified | Medical Devices & Rad Health | 1291380 |
| October 10, 2024 | Not classified | Medical Devices & Rad Health | 1252230 |
| September 13, 2023 | Not classified | Medical Devices & Rad Health | 1219683 |
| August 28, 2019 | Not classified | Medical Devices & Rad Health | 1104689 |
| August 14, 2018 | Not classified | Medical Devices & Rad Health | 1063309 |
| September 12, 2017 | Not classified | Medical Devices & Rad Health | 1026230 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
PENRAD at Sisters Grove Pavilion
FEI Number
3007174651
Address
6001 E Woodmen Rd Ste 10, Colorado Springs, CO 80923-2601, United States
Country
United States
ID: 05e1f8e9-baa9-4936-8bed-2ee49b6b17de