PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma
FDA inspection history in Greenville, South Carolina, 2015 to 2023
- 3
- Form 483s
Every document, by year
- Form 483
2015: one Form 483; 2019: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Greenville, South Carolina.
- 2019One Form 483, at Greenville, South Carolina.
- 2019The longest 483 on file: 4 observations over 5 pages at Greenville, South Carolina.
- 2023One Form 483, at Greenville, South Carolina.
Cited most
Across all PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma observations on file
- 21 CFR 314.80(b)Postmarketing reporting of adverse drug experiences2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma 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
Greenville, South Carolina
Three Form 483s · 2015 to 2023 · 8 observations
Latest: Form 483, Aug 2, 2023 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-08-02 | 483 Form 483 | Greenville, South Carolina | 2 | $99 |
| 2019-02-22 | 483 Form 483 | Greenville, South Carolina | 4 | $99 |
| 2015-08-20 | 483 Form 483 | Greenville, South Carolina | 2 | $99 |
Investigators on these documents
FEI number 1017687 · most recent document Aug 2, 2023
About PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma
How many FDA Form 483s has PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma received?
FDA Intel has 3 Form 483s on file for PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma; the most recent is dated Aug 2, 2023.
When was PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma last inspected by FDA?
The most recent FDA inspection document on file for PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma is a Form 483 dated Aug 2, 2023, for the site in Greenville, South Carolina.
What did FDA cite at PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma?
The regulations cited most in the observations on file for PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma are 21 CFR 314.80(b) (Postmarketing reporting of adverse drug experiences), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.