DPT Laboratories, Ltd
FDA inspection history in San Antonio, Texas, 2018 to 2020
- 2
- Form 483s
Every document, by year
- Form 483
2018: one amended 483; 2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018–20One amended 483 and one Form 483, at San Antonio, Texas.
- 2020The longest 483 on file: 6 observations over 4 pages at San Antonio, Texas.
Cited most
Across all DPT Laboratories observations on file
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.160General requirements1
- 21 CFR 211.182Equipment cleaning and use log1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.192Production record review1
The complete DPT Laboratories 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
San Antonio, Texas
One Form 483 and one amended 483 · 2018 to 2020 · 7 observations
Latest: Form 483, Feb 7, 2020 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-02-07 | 483 Form 483 | San Antonio, Texas | 6 | $99 |
| 2018-12-14 | Amended 483 Amended 483 | San Antonio, Texas | 1 | $99 |
Investigators on these documents
FEI number 1628114 · most recent document Feb 7, 2020
About DPT Laboratories, Ltd
How many FDA Form 483s has DPT Laboratories, Ltd received?
FDA Intel has 2 Form 483s on file for DPT Laboratories, Ltd; the most recent is dated Feb 7, 2020.
When was DPT Laboratories, Ltd last inspected by FDA?
The most recent FDA inspection document on file for DPT Laboratories, Ltd is a Form 483 dated Feb 7, 2020, for the site in San Antonio, Texas.
What did FDA cite at DPT Laboratories, Ltd?
The regulations cited most in the observations on file for DPT Laboratories, Ltd are 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.182 (Equipment cleaning and use log), 1 time.