Trinity Sterile, Inc.
FDA inspection history in Salisbury, Maryland, 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 Salisbury, Maryland.
Cited most
Across all Trinity Sterile observations on file
- 21 CFR 820.75(a)Process validation1
- 21 CFR 820.90(a)Nonconforming product1
The complete Trinity Sterile file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Salisbury, Maryland
One Form 483 · 2017 · 2 observations
Latest: Form 483, Mar 13, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-03-13 | 483 Form 483 | Salisbury, Maryland | 2 | $99 |
Investigators on these documents
FEI number 1000123297 · most recent document Mar 13, 2017
About Trinity Sterile, Inc.
How many FDA Form 483s has Trinity Sterile, Inc. received?
FDA Intel has 1 Form 483 on file for Trinity Sterile, Inc.; the most recent is dated Mar 13, 2017.
When was Trinity Sterile, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Trinity Sterile, Inc. is a Form 483 dated Mar 13, 2017, for the site in Salisbury, Maryland.
What did FDA cite at Trinity Sterile, Inc.?
The regulations cited most in the observations on file for Trinity Sterile, Inc. are 21 CFR 820.75(a) (Process validation), 1 time; 21 CFR 820.90(a) (Nonconforming product), 1 time.