Pharmadepot Labs, LLC
FDA inspection history in San Diego, California, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at San Diego, California.
Cited most
Across all Pharmadepot Labs observations on file
- 21 CFR 211.160(b)General requirements2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
The complete Pharmadepot Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Diego, California
One Form 483 · 2024 · 5 observations
Latest: Form 483, Jun 18, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-06-18 | 483 Form 483 | San Diego, California | 5 | $99 |
Investigators on these documents
FEI number 3017534691 · most recent document Jun 18, 2024
About Pharmadepot Labs, LLC
How many FDA Form 483s has Pharmadepot Labs, LLC received?
FDA Intel has 1 Form 483 on file for Pharmadepot Labs, LLC; the most recent is dated Jun 18, 2024.
When was Pharmadepot Labs, LLC last inspected by FDA?
The most recent FDA inspection document on file for Pharmadepot Labs, LLC is a Form 483 dated Jun 18, 2024, for the site in San Diego, California.
What did FDA cite at Pharmadepot Labs, LLC?
The regulations cited most in the observations on file for Pharmadepot Labs, LLC are 21 CFR 211.160(b) (General requirements), 2 times; 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.