Parker Laboratories, Inc
FDA inspection history in Fairfield, New Jersey, 2018 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Fairfield, New Jersey.
- 2023One Form 483, at Fairfield, New Jersey.
- 2023The longest 483 on file: 5 observations over 3 pages at Fairfield, New Jersey.
Cited most
Across all Parker Laboratories observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.188(b)(7)Batch production and control records1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Parker 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
Fairfield, New Jersey
Two Form 483s · 2018 to 2023 · 8 observations
Latest: Form 483, Jun 14, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-06-14 | 483 Form 483 | Fairfield, New Jersey | 5 | $99 |
| 2018-03-20 | 483 Form 483 | Fairfield, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 2212018 · most recent document Jun 14, 2023
About Parker Laboratories, Inc
How many FDA Form 483s has Parker Laboratories, Inc received?
FDA Intel has 2 Form 483s on file for Parker Laboratories, Inc; the most recent is dated Jun 14, 2023.
When was Parker Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Parker Laboratories, Inc is a Form 483 dated Jun 14, 2023, for the site in Fairfield, New Jersey.
What did FDA cite at Parker Laboratories, Inc?
The regulations cited most in the observations on file for Parker Laboratories, Inc are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.180(e)(2) (General requirements), 1 time.