DPT Laboratories, Ltd.
FDA inspection history in San Antonio, Texas, 2014 to 2023
- 3
- Form 483s
Every document, by year
- Form 483
2014: one Form 483; 2016: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014–16Two Form 483s, at San Antonio, Texas.
- 2014The longest 483 on file: 7 observations over 4 pages at San Antonio, Texas.
- 2023One Form 483, at San Antonio, Texas.
Cited most
Across all DPT Laboratories observations on file
- 21 CFR 211.122(a)Materials examination and usage criteria3
- 21 CFR 211.100(b)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194(a)Laboratory records1
The complete DPT Laboratories 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
San Antonio, Texas
Three Form 483s · 2014 to 2023 · 11 observations
Latest: Form 483, Apr 6, 2023 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-04-06 | 483 Form 483 | San Antonio, Texas | 1 | $99 |
| 2016-08-26 | 483 Form 483 | San Antonio, Texas | 3 | $99 |
| 2014-04-25 | 483 Form 483 | San Antonio, Texas | 7 | $99 |
Investigators on these documents
Ademola O. Daramola (1)Camerson E. Moore (1)Gilbert Valdez (1)Jason R. Caballero (1)
FEI number 1000117684 · most recent document Apr 6, 2023
About DPT Laboratories, Ltd.
How many FDA Form 483s has DPT Laboratories, Ltd. received?
FDA Intel has 3 Form 483s on file for DPT Laboratories, Ltd.; the most recent is dated Apr 6, 2023.
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 Apr 6, 2023, 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 211.122(a) (Materials examination and usage criteria), 3 times; 21 CFR 211.100(b) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.