Seniorlife Technologies Inc.
FDA inspection history in Bellevue, Washington, 2025 to 2026
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Form 483
- Warning letter
2025: one warning letter; 2026: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2025–26Two Form 483s and one warning letter, at Bellevue, Washington.
- 2026The longest 483 on file: 7 observations over 6 pages at Bellevue, Washington.
Cited most
Across all Seniorlife Technologies observations on file
- 21 CFR 820.10Requirements for a quality management system4
- 21 CFR 830.300Devices subject to device identification data submission requirements2
- 21 CFR 820.180General requirements1
- 21 CFR 820.20Management responsibility1
- 21 CFR 820.22Quality audit1
The complete Seniorlife Technologies file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Bellevue, Washington
Two Form 483s and one warning letter · 2025 to 2026 · 13 observations
Latest: Form 483, Feb 20, 2026 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-20 | 483 Form 483 | Bellevue, Washington | 7 | $99 |
| 2026-02-20 | 483 Form 483 | Bellevue, Washington | 6 | $99 |
| 2025-08-21 | Warning letter Warning letter | Bellevue, Washington | — | $99 |
Investigators on these documents
FEI number 3027535342 · most recent document Feb 20, 2026
About Seniorlife Technologies Inc.
How many FDA Form 483s has Seniorlife Technologies Inc. received?
FDA Intel has 2 Form 483s on file for Seniorlife Technologies Inc.; the most recent is dated Feb 20, 2026.
When was Seniorlife Technologies Inc. last inspected by FDA?
The most recent FDA inspection document on file for Seniorlife Technologies Inc. is a Form 483 dated Feb 20, 2026, for the site in Bellevue, Washington.
What did FDA cite at Seniorlife Technologies Inc.?
The regulations cited most in the observations on file for Seniorlife Technologies Inc. are 21 CFR 820.10 (Requirements for a quality management system), 4 times; 21 CFR 830.300 (Devices subject to device identification data submission requirements), 2 times; 21 CFR 820.180 (General requirements), 1 time.
Has Seniorlife Technologies Inc. received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Seniorlife Technologies Inc.; the most recent is dated Aug 21, 2025.