Triaid, Inc.
Form 483 issued June 3, 2016 · Cumberland, Maryland
- Inspection
- May 25 – Jun 3, 2016
- Investigator
- Cynthia A. Harris
- Observations
- 2
- Pages
- 2
- FEI number
- 3000204844
In short: On June 3, 2016, FDA issued a Form 483 with 2 observations to Triaid, Inc. in Cumberland, Maryland (FEI 3000204844) after an inspection that ran May 25 – Jun 3, 2016. The investigator was Cynthia A. Harris. Most observations concern cAPA; the most-cited regulation is 21 CFR 820.198 (complaint files).
At a glance
Observations span 1 system, led by capa.
Most cited: 21 CFR 820.198(a) (1×)
What FDA observed
Preview: the opening words of each observation- 01
Procedures for receiving, reviewing, and evaluating complaints by a formally designated unit…
- 02
: Promised to…
This inspection in context
Cynthia A. Harris
2 documents · 2015–2016
Cites 58.33 (study director) more than any other section. Most of their documents are for sites in Maryland.
The firmTriaid, Inc. history
The site's inspection history, in date order.
Similar 483sOther sites cited under 820.198(a)
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Triaid, Inc.?
FDA listed 2 observations on this Form 483, mostly about cAPA. The most-cited regulation is 21 CFR 820.198 (complaint files). The opening words of each observation are shown on this page.
Who inspected Triaid, Inc.?
Cynthia A. Harris is named on this Form 483, for the inspection of May 25 – Jun 3, 2016. Each investigator has a profile showing what they cite most.
When was Triaid, Inc. inspected by FDA?
The inspection ran May 25 – Jun 3, 2016, and the Form 483 is dated June 3, 2016.
How do I get the full Form 483 for Triaid, Inc.?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.