VistaPharm, Inc.
FDA inspection history in Largo, Florida, 2015 to 2022
- 3
- Form 483s
Every document, by year
- Form 483
2015: one Form 483; 2018: one Form 483; 2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Largo, Florida.
- 2015The longest 483 on file: 10 observations over 10 pages at Largo, Florida.
- 2018One Form 483, at Largo, Florida.
- 2022One Form 483, at Largo, Florida.
Cited most
Across all VistaPharm observations on file
- 21 CFR 211.100Written procedures; deviations3
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.160General requirements1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.180General requirements1
The complete VistaPharm 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
Largo, Florida
Three Form 483s · 2015 to 2022 · 15 observations
Latest: Form 483, Sep 2, 2022 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-02 | 483 Form 483 | Largo, Florida | 3 | $99 |
| 2018-01-16 | 483 Form 483 | Largo, Florida | 2 | $99 |
| 2015-05-28 | 483 Form 483 | Largo, Florida | 10 | $99 |
Investigators on these documents
Damaris Y. Hernandez (1)Jessica L. Pressley (1)Nicole E. Knowlton (1)Oes C. Iy (1)Steven A. Brettler (1)
FEI number 1036352 · most recent document Sep 2, 2022
About VistaPharm, Inc.
How many FDA Form 483s has VistaPharm, Inc. received?
FDA Intel has 3 Form 483s on file for VistaPharm, Inc.; the most recent is dated Sep 2, 2022.
When was VistaPharm, Inc. last inspected by FDA?
The most recent FDA inspection document on file for VistaPharm, Inc. is a Form 483 dated Sep 2, 2022, for the site in Largo, Florida.
What did FDA cite at VistaPharm, Inc.?
The regulations cited most in the observations on file for VistaPharm, Inc. are 21 CFR 211.100 (Written procedures; deviations), 3 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.160 (General requirements), 1 time.