Spok, Inc
FDA inspection history in Alexandria, Virginia, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Alexandria, Virginia.
Cited most
Across all Spok observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.70(a)Production and process controls1
The complete Spok file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Alexandria, Virginia
One Form 483 · 2024 · 4 observations
Latest: Form 483, Jul 19, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-07-19 | 483 Form 483 | Alexandria, Virginia | 4 | $99 |
Investigators on these documents
FEI number 3014158829 · most recent document Jul 19, 2024
About Spok, Inc
How many FDA Form 483s has Spok, Inc received?
FDA Intel has 1 Form 483 on file for Spok, Inc; the most recent is dated Jul 19, 2024.
When was Spok, Inc last inspected by FDA?
The most recent FDA inspection document on file for Spok, Inc is a Form 483 dated Jul 19, 2024, for the site in Alexandria, Virginia.
What did FDA cite at Spok, Inc?
The regulations cited most in the observations on file for Spok, Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.22 (Quality audit), 1 time; 21 CFR 820.50 (Purchasing controls), 1 time.