Straight Arrow Products, Inc.
FDA inspection history in Easton, Pennsylvania, 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 Easton, Pennsylvania.
Cited most
Across all Straight Arrow Products observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.180(e)(1)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(b)(3)Equipment cleaning and maintenance1
The complete Straight Arrow Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Easton, Pennsylvania
One Form 483 · 2024 · 6 observations
Latest: Form 483, Oct 15, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-15 | 483 Form 483 | Easton, Pennsylvania | 6 | $99 |
Investigators on these documents
FEI number 3014727651 · most recent document Oct 15, 2024
About Straight Arrow Products, Inc.
How many FDA Form 483s has Straight Arrow Products, Inc. received?
FDA Intel has 1 Form 483 on file for Straight Arrow Products, Inc.; the most recent is dated Oct 15, 2024.
When was Straight Arrow Products, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Straight Arrow Products, Inc. is a Form 483 dated Oct 15, 2024, for the site in Easton, Pennsylvania.
What did FDA cite at Straight Arrow Products, Inc.?
The regulations cited most in the observations on file for Straight Arrow Products, Inc. are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.180(e)(1) (General requirements), 1 time.