Hayward Laboratories, Inc.
FDA inspection history in E Stroudsburg, Pennsylvania, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at E Stroudsburg, Pennsylvania.
Cited most
Across all Hayward Laboratories observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.165(e)Testing and release for distribution1
- 21 CFR 211.166(b)Stability testing1
- 21 CFR 211.198(a)Complaint files1
The complete Hayward Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
E Stroudsburg, Pennsylvania
One Form 483 · 2017 · 9 observations
Latest: Form 483, Jul 20, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-07-20 | 483 Form 483 | E Stroudsburg, Pennsylvania | 9 | $99 |
Investigators on these documents
FEI number 2220345 · most recent document Jul 20, 2017
About Hayward Laboratories, Inc.
How many FDA Form 483s has Hayward Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for Hayward Laboratories, Inc.; the most recent is dated Jul 20, 2017.
When was Hayward Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Hayward Laboratories, Inc. is a Form 483 dated Jul 20, 2017, for the site in E Stroudsburg, Pennsylvania.
What did FDA cite at Hayward Laboratories, Inc.?
The regulations cited most in the observations on file for Hayward Laboratories, Inc. are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.165(e) (Testing and release for distribution), 1 time.