SOFTAP INC
FDA inspection history in Livermore, California, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Livermore, California.
Cited most
Across all SOFTAP observations on file
- 21 CFR 211.150Distribution procedures1
- 21 CFR 211.170(b)Reserve samples1
- 21 CFR 211.180(e)General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.198(a)Complaint files1
The complete SOFTAP file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Livermore, California
One Form 483 · 2023 · 7 observations
Latest: Form 483, Dec 11, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-12-11 | 483 Form 483 | Livermore, California | 7 | $99 |
Investigators on these documents
FEI number 3013155761 · most recent document Dec 11, 2023
About SOFTAP INC
How many FDA Form 483s has SOFTAP INC received?
FDA Intel has 1 Form 483 on file for SOFTAP INC; the most recent is dated Dec 11, 2023.
When was SOFTAP INC last inspected by FDA?
The most recent FDA inspection document on file for SOFTAP INC is a Form 483 dated Dec 11, 2023, for the site in Livermore, California.
What did FDA cite at SOFTAP INC?
The regulations cited most in the observations on file for SOFTAP INC are 21 CFR 211.150 (Distribution procedures), 1 time; 21 CFR 211.170(b) (Reserve samples), 1 time; 21 CFR 211.180(e) (General requirements), 1 time.