Avista Pharma Solutions, Inc. dba
FDA inspection history in Agawam, Massachusetts, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Agawam, Massachusetts.
Cited most
Across all Avista Pharma Solutions, Inc. dba observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Avista Pharma Solutions, Inc. dba file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Agawam, Massachusetts
One Form 483 · 2019 · 2 observations
Latest: Form 483, Dec 18, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-12-18 | 483 Form 483 | Agawam, Massachusetts | 2 | $99 |
Investigators on these documents
FEI number 1220785 · most recent document Dec 18, 2019
About Avista Pharma Solutions, Inc. dba
How many FDA Form 483s has Avista Pharma Solutions, Inc. dba received?
FDA Intel has 1 Form 483 on file for Avista Pharma Solutions, Inc. dba; the most recent is dated Dec 18, 2019.
When was Avista Pharma Solutions, Inc. dba last inspected by FDA?
The most recent FDA inspection document on file for Avista Pharma Solutions, Inc. dba is a Form 483 dated Dec 18, 2019, for the site in Agawam, Massachusetts.
What did FDA cite at Avista Pharma Solutions, Inc. dba?
The regulations cited most in the observations on file for Avista Pharma Solutions, Inc. dba are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.67(a) (Equipment cleaning and maintenance), 1 time.