Medical Products Laboratories, Inc
FDA inspection history in Philadelphia, Pennsylvania, 2015 to 2026
- 4
- Form 483s
- 1
- Warning letter
Every document, by year
- Warning letter
- Form 483
2015: one Form 483; 2017: one Form 483; 2020: one Form 483; 2023: one Form 483; 2026: one warning letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2015–17Two Form 483s, at Philadelphia, Pennsylvania.
- 2017The longest 483 on file: 8 observations over 9 pages at Philadelphia, Pennsylvania.
- 2020One Form 483, at Philadelphia, Pennsylvania.
- 2023One Form 483, at Philadelphia, Pennsylvania.
- 2026One warning letter, at Philadelphia, Pennsylvania.
Cited most
Across all Medical Products Laboratories observations on file
- 21 CFR 211.160General requirements5
- 21 CFR 211.194Laboratory records4
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Medical Products Laboratories file.
All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
15% off buying them one by one
Sites
Philadelphia, Pennsylvania
Four Form 483s and one warning letter · 2015 to 2026 · 17 observations
Latest: Warning letter, Apr 9, 2026 →
Documents
5 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-04-09 | Warning letter Warning letter | Philadelphia, Pennsylvania | — | $99 |
| 2023-07-13 | 483 Form 483 | Philadelphia, Pennsylvania | 1 | $99 |
| 2020-03-13 | 483 Form 483 | Philadelphia, Pennsylvania | 5 | $99 |
| 2017-10-12 | 483 Form 483 | Philadelphia, Pennsylvania | 8 | $99 |
| 2015-07-21 | 483 Form 483 | Philadelphia, Pennsylvania | 3 | $99 |
Investigators on these documents
Alison N. Correll (1)Christina K. Theodorou (1)Daniel J. Min (1)Junho Pak (1)Michael A. Taylor (1)Rachael O. Oyewole (1)Sam Pepe (1)
FEI number 2513595 · most recent document Apr 9, 2026
About Medical Products Laboratories, Inc
How many FDA Form 483s has Medical Products Laboratories, Inc received?
FDA Intel has 4 Form 483s on file for Medical Products Laboratories, Inc; the most recent is dated Jul 13, 2023.
When was Medical Products Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Medical Products Laboratories, Inc is a Form 483 dated Jul 13, 2023, for the site in Philadelphia, Pennsylvania.
What did FDA cite at Medical Products Laboratories, Inc?
The regulations cited most in the observations on file for Medical Products Laboratories, Inc are 21 CFR 211.160 (General requirements), 5 times; 21 CFR 211.194 (Laboratory records), 4 times; 21 CFR 211.100 (Written procedures; deviations), 2 times.
Has Medical Products Laboratories, Inc received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Medical Products Laboratories, Inc; the most recent is dated Apr 9, 2026.