Belcher Pharmaceuticals, LLC
FDA inspection history in Largo, Florida, 2016 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Largo, Florida.
- 2016The longest 483 on file: 9 observations over 14 pages at Largo, Florida.
- 2024One Form 483, at Largo, Florida.
Cited most
Across all Belcher Pharmaceuticals observations on file
- 21 CFR 211.160General requirements3
- 21 CFR 211.167Special testing requirements2
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.165Testing and release for distribution1
The complete Belcher Pharmaceuticals file.
All 2 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
Two Form 483s · 2016 to 2024 · 15 observations
Latest: Form 483, Aug 16, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-08-16 | 483 Form 483 | Largo, Florida | 6 | $99 |
| 2016-05-13 | 483 Form 483 | Largo, Florida | 9 | $99 |
Investigators on these documents
Jennifer Lalama (1)Jessica L. Pressley (1)Jessica P. McAlister (1)Kayla V. Sprague (1)Miguel A. Martinez (1)Stephanie D. Crockett (1)
FEI number 1000526113 · most recent document Aug 16, 2024
About Belcher Pharmaceuticals, LLC
How many FDA Form 483s has Belcher Pharmaceuticals, LLC received?
FDA Intel has 2 Form 483s on file for Belcher Pharmaceuticals, LLC; the most recent is dated Aug 16, 2024.
When was Belcher Pharmaceuticals, LLC last inspected by FDA?
The most recent FDA inspection document on file for Belcher Pharmaceuticals, LLC is a Form 483 dated Aug 16, 2024, for the site in Largo, Florida.
What did FDA cite at Belcher Pharmaceuticals, LLC?
The regulations cited most in the observations on file for Belcher Pharmaceuticals, LLC are 21 CFR 211.160 (General requirements), 3 times; 21 CFR 211.167 (Special testing requirements), 2 times; 21 CFR 211.194 (Laboratory records), 2 times.