Nova-Tech, Inc.
FDA inspection history in Grand Island, Nebraska, 2022 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022–23Two Form 483s, at Grand Island, Nebraska.
- 2022The longest 483 on file: 7 observations over 10 pages at Grand Island, Nebraska.
Cited most
Across all Nova-Tech observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
The complete Nova-Tech 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
Grand Island, Nebraska
Two Form 483s · 2022 to 2023 · 9 observations
Latest: Form 483, May 12, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-12 | 483 Form 483 | Grand Island, Nebraska | 2 | $99 |
| 2022-03-15 | 483 Form 483 | Grand Island, Nebraska | 7 | $99 |
Investigators on these documents
FEI number 1931182 · most recent document May 12, 2023
About Nova-Tech, Inc.
How many FDA Form 483s has Nova-Tech, Inc. received?
FDA Intel has 2 Form 483s on file for Nova-Tech, Inc.; the most recent is dated May 12, 2023.
When was Nova-Tech, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Nova-Tech, Inc. is a Form 483 dated May 12, 2023, for the site in Grand Island, Nebraska.
What did FDA cite at Nova-Tech, Inc.?
The regulations cited most in the observations on file for Nova-Tech, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.